Category: 680-65-9

680-65-9, A common compound: 680-65-9, name is Diethyl difluoromalonate, belongs to esters-buliding-blocks compound, it can change the direction of chemical reaction, and react with certain compounds to generate new functional products. A new synthetic method of this compound is introduced below.

5 g (1.0 eq., 25.49 mmol) of the compound 37 was dissolved in 40 mL of methanol, and 30 mL of methanol solution of sodium hydroxide (1.43 g (1.0 eq., 25.49 mmol)) was added dropwise thereto. It was then stirred for 3 hours at room temperature. After confirming by TLC the disappearance of the reacting materials, benzyl amine (8.4 mL (3.0 eq., 76.47 mmol)) was added and stirred overnight at 55 C. The reaction solution was concentrated under reduced pressure by using an evaporator, and the precipitated solids were added with diethyl ether followed by washing and filtering. The washed solids were dissolved in 1 M HCl. Then, liquid fractionation extraction was performed 3 times using ethyl acetate. The collected organic layer was washed with a saturated aqueous solution of NaCl. After drying over magnesium sulfate, it was concentrated under reduced pressure by using an evaporator in water bath at 40 C. to obtain the residues (compound 39). It was directly subjected to the following reducing reaction.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Diethyl difluoromalonate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Seikagaku Corporation; Miyamoto, Kenji; Yasuda, Yosuke; Takeuchi, Hisayuki; Yoshioka, Keiji; (69 pag.)US2016/151506; (2016); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Synthetic Route of 680-65-9, A common heterocyclic compound, 680-65-9, name is Diethyl difluoromalonate, molecular formula is C7H10F2O4, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Step 1: 2,2-difluoropropane-1,3-diol To a solution of diethyl difluoromalonate (3.77 g, 19.22 mmol) in THF (19.22 ml) at 0 C., was added Lithium Aluminium Hydride (1M in THF, 30.8 ml, 30.8 mmol) drop-wise. The reaction mixture was brought to ambient temperature and then stirred for 16 hours. The reaction mixture was then slowly poured onto an ice-cold suspension of 4 g of Na2SO4.10H2O in 20 mL of THF. This was stirred for 1 h and the resulting slurry was filtered, rinsed with 1:3 MeOH/EtOAc. The filtrate was collected and concentrated to give the title compound (1.7 g, 15.17 mmol, 79% yield) as a white paste.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; LEWIS, Richard T.; ALLEN, Jennifer R.; CHENG, Yuan; CHOQUETTE, Deborah; EPSTEIN, Oleg; GUZMAN-PEREZ, Angel; HARRINGTON, Paul E.; HUA, Zihao; HUNGATE, Randall W.; HUMAN, Jason Brooks; JUDD, Ted; LIU, Qingyian; LOPEZ, Patricia; MINATTI, Ana Elena; OLIVIERI, Philip; ROMERO, Karina; RUMFELT, Shannon; RZASA, Robert M.; SCHENKEL, Laurie; STELLWAGEN, John; WHITE, Ryan; XUE, Qiufen; ZHENG, Xiao; ZHONG, Wenge; US2014/107109; (2014); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Electric Literature of 680-65-9,Some common heterocyclic compound, 680-65-9, name is Diethyl difluoromalonate, molecular formula is C7H10F2O4, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

In a dry 25 mL round bottom flask under an Ar atmosphere, NaOEt (9.71 mL, 26.0mmol) in EtOH (21 % weight) and diethyl-2,2-difluoromalonate (2.55 g, 13.0 mmol) werestirred at rt for 10 mm. A solution of Example id (554 mg, 1.30 mmol) in EtOH (6.00mL) was added dropwise and the reaction was stirred at rt over 18 hrs. The EtOH wasremoved in vacuo and the crude oil was dissolved in 1 M HC1 (10 mL). The aqueoussolution was extracted with EtOAc (20 mL x 3), and the combined organics were washedwith aq NaC1 (20 mL), dried over Na2SO4, filtered into a round bottom flask andconcentrated in vacuo to give the title compound as a crude brown oil (749 mg, 1.30mmol). MS (ESI) 576.0 [M+H]+.

The synthetic route of 680-65-9 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; BRISTOL-MYERS SQUIBB COMPANY; EXELIXIS PATENT COMPANY LLC; KICK, Ellen, K.; BODAS, Mandar; MOHAN, Raju; BUSCH, Brett, B.; AVERBUJ, Claudia; VALENTE, Meriah; WURTZ, Nicholas; RAO, Prasanna Savanor, Maddu; SHETTY, Jeevanprakash; VENU, Alla; WO2014/152738; (2014); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Electric Literature of 680-65-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 680-65-9, name is Diethyl difluoromalonate belongs to esters-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

A SOLUTION OF COMMERCIALLY AVAILABLE DIETHYL DIFLUOROMALONATE (10.1145 g, 0.0515 mol) in anhydrous methanol (110 mL) was saturated with ammonia (g) at 0 C for 45 min. The resulting mixture was stirred in an ice bath for 3h and monitored by MS (m/z M+H 139). The product was concentrated under reduced pressure to afford desired amide 13-2 as a white powder (7.1027 g, 99%): HR-MS (ES) m/z CALCD FOR C3H4N2F202 (MH+) =139. 0314. Observed: 139.0278.

The synthetic route of Diethyl difluoromalonate has been constantly updated, and we look forward to future research findings.

Reference:
Patent; PHARMACIA CORPRATION; WO2004/60376; (2004); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 680-65-9, name is Diethyl difluoromalonate, A new synthetic method of this compound is introduced below., SDS of cas: 680-65-9

Diethyl difluoropropanedioate (2.87 ml, 17.23 mmol) was dissolved in MeOH (20 mL) and a solution of 2,3-dihvdro-1H-inden-2-ainine (2.07 g, 15.51 mmol) in MeOH (15mL) was added dropwise. The reaction was stirred at RT for 14 h. The reaction wasconcentrated and purified by Biotage FCC (50 g SNAP KP-Si02, 0-50% EtOAc in Heptanes)affording the title compound as a pale brown solid (1.79 g, 91% purity, 35%)?H NMR (500 MHz, DMSO-d6) 9.48 (d, J = 6.9 Hz, 1H), 7.22 (dcl, J = 5.3, 3.4 Hz,2H), 7.15 (dd, J = 5.5, 3.2 Hz, 2H), 4.60-4.48 (in, IH). 3.88 (s, 3H), 3.20 (dd, .J= 15.9, 7.9Hz, 2H), 2.91 (dd, J= 15.9, 6.6 Hz, 2H). LCMS Method C: rt 1.09 mm, 91%, m/z 269.95(MW)

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; PRESIDENT AND FELLOWS OF HARVARD COLLEGE; EVOTEC INTERNATIONAL GMBH; GAMPE, Christian, M.; KAHNE, Daniel, Evan; KAHNE, Suzanne, Walker; QIAO, Yuan; EAST, Stephen; PARKES, Alastair, L.; SOUTHEY, Michelle; HUNTER, James; WHITTAKER, Mark; ARTHUIS, Martin; (359 pag.)WO2016/191658; (2016); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Electric Literature of 680-65-9, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 680-65-9, name is Diethyl difluoromalonate, This compound has unique chemical properties. The synthetic route is as follows.

EXAMPLE 152. Preparation of 4-((lR,3aS,5aR,5bR,7aR,llaS,llbR,13aR,13bR)-3a ((3-(2-(dimethylamino)ethylamino)-2,2-difluoro-3-oxopropanamido)methyl)- 5a,5b,8,8, 11 a-pentamethyl- 1 -(prop- 1 -en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,ll,lla,llb,12,13,13a,13b-octadecahydro-lH- cyclopenta[a]chrysen-9-yl)benzoic acid. Step 1: Preparation of the C28 reversed amide To a solution of tert-butyl 4-((lR,3aS,5aR,5bR,7aR,l laS,l lbR,13aR,13bR)-3a- (aminomethyl)-5a,5b,8,8, 11 a-pentamethyl-1 -(prop- 1 -en-2-yl)- 2,3,3a,4,5,5a,5b,6,7,7a,8,l l,l la,l lb,12,13,13a,13b-octadecahydro-lH- cyclopenta[a]chrysen-9-yl)benzoate (200 mg, 0.333 mmol) in methanol (5 ml) and 1,4-dioxane (5 ml) was added diethyl 2,2-difluoromalonate (654 mg, 3.33 mmol). The resulting solution was stirred at rt for 6 days. The reaction mixture was concentrated in vacuo. The crude product was purified by Biotage (Thomson 25 g silica gel column; 4: 1 Hex/EtOAc) to give 116 mg (47 %) of product. MS: m/e 736.6 (MH+), 2.86 min (method 2). ? NMR (400 MHz, CHLOROFORM-d) delta ppm 0.93 (s, 6 H) 0.99 (s, 3 H) 1.02 (s, 3 H) 1.13 (s, 3 H) 1.60 (s, 9 H) 1.71 (s, 3 H) 0.85 – 1.83 (20 H) 1.98 – 2.10 (m, 1 H) 2.10 (dd, J=17.07, 6.27 Hz, 1 H) 2.49 (td, J=l 1.04, 5.27 Hz, 1 H) 3.16 (dd, J=13.55, 6.27 Hz, 1 H) 3.65 (dd, J=14.43, 7.15 Hz, 1 H) 3.95 (s, 3 H) 4.61 – 4.65 (m, 1 H) 4.73 (d, J=1.76 Hz, 1 H) 5.28 (dd, J=6.15, 1.63 Hz, 1 H) 6.28 (t, J=7.03 Hz, 1 H) 7.18 (d, J=8.53 Hz, 2 H) 7.89 (d, J=8.28 Hz, 2 H). iyF NMR (376 MHz, CHLOROFORM-d) delta ppm -112.49 (s, 2 F).

The chemical industry reduces the impact on the environment during synthesis Diethyl difluoromalonate. I believe this compound will play a more active role in future production and life.

Reference:
Patent; BRISTOL-MYERS SQUIBB COMPANY; REGUEIRO-REN, Alicia; SWIDORSKI, Jacob; SIT, Sing-Yuen; CHEN, Yan; CHEN, Jie; MEANWELL, Nicholas A.; LIU, Zheng; WO2012/106188; (2012); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

680-65-9, A common compound: 680-65-9, name is Diethyl difluoromalonate, belongs to esters-buliding-blocks compound, it can change the direction of chemical reaction, and react with certain compounds to generate new functional products. A new synthetic method of this compound is introduced below.

5 g (1.0 eq., 25.49 mmol) of the compound 37 was dissolved in 40 mL of methanol, and 30 mL of methanol solution of sodium hydroxide (1.43 g (1.0 eq., 25.49 mmol)) was added dropwise thereto. It was then stirred for 3 hours at room temperature. After confirming by TLC the disappearance of the reacting materials, benzyl amine (8.4 mL (3.0 eq., 76.47 mmol)) was added and stirred overnight at 55 C. The reaction solution was concentrated under reduced pressure by using an evaporator, and the precipitated solids were added with diethyl ether followed by washing and filtering. The washed solids were dissolved in 1 M HCl. Then, liquid fractionation extraction was performed 3 times using ethyl acetate. The collected organic layer was washed with a saturated aqueous solution of NaCl. After drying over magnesium sulfate, it was concentrated under reduced pressure by using an evaporator in water bath at 40 C. to obtain the residues (compound 39). It was directly subjected to the following reducing reaction.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Diethyl difluoromalonate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Seikagaku Corporation; Miyamoto, Kenji; Yasuda, Yosuke; Takeuchi, Hisayuki; Yoshioka, Keiji; (69 pag.)US2016/151506; (2016); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

A common heterocyclic compound, 680-65-9, name is Diethyl difluoromalonate, molecular formula is C7H10F2O4, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. 680-65-9.

Step 1: Procedure for preparation of Compound 9bTo a solution of NH3/MeOH (sat., 50 mL) was added compound 9a (5 g, 25.5 mmol) at -78 C and stirred at this temperature for 2 h. Then the reaction mixture was allowed to warm to room temperature slowly and stirred overnight. The reaction mixture was concentrated under reduced pressure to dryness to give compound 9b (3.3 g, 94%) as a white solid.1H NMR (DMSO-dtf 400 MHz): delta 8.24 (br, 2H), 8.09 (br, 2H).

The synthetic route of Diethyl difluoromalonate has been constantly updated, and we look forward to future research findings.

Reference:
Patent; DILLARD, Lawrence W.; YUAN, Jing; LEFTHERIS, Katerina; VENKATRAMAN, Shankar; WU, Guosheng; JIA, Lanqi; XU, Zhenrong; CACATIAN, Salvacion; MORALES-RAMOS, Angel; SINGH, Suresh; ZHENG, Yajun; WO2011/106414; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics