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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400990Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → Diethyl 2,2-difluoropentanedioate

https://huagongshe.com/reaction/400990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantEthyl AcrylateHCID 8821—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl bromodifluoroacetateHCID 69585—
CatalystCopperHCID 23978—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductDiethyl 2,2-difluoropentanedioateHCID 20455495299.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl bromodifluoroacetate (33.2 g) in tetrahydrofuran (94.0 g) was added ethyl acrylate (8.2 g) and copper powder (10.9 g). After heating to 50° C., TMEDA (9.5 g) was added dropwise and the reaction mixture was then stirred for 3 hours at the same temperature. Upon disappearance of ethyl acrylate as the starting material, to the reaction solution was added methyl t-butyl ether (MTBE, 73.7 g) followed by addition of 10% aqueous ammonium chloride solution (49.8 g) dropwise, and the mixture was then stirred for 30 minutes. The remaining copper residue was removed by filtration through a celite, and methyl t-butyl ether (MTBE, 66.3 g) was added to separate the layers. The separated organic layer was washed successively with 10% aqueous NH4Cl solution (66.3 g) and 3 N aqueous hydrochloric acid solution (99.6 g) in order and then distilled under reduced pressure to obtain 55.0 g of the desired title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741927B2
Source datasetuspto-grants-2014_06
ORD IDord-d94d99c1ee2a4b8f867711415bd0060a
Source noteuspto-grants-2014_06