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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929271Generated: October 30, 2026

Chloroform → 1-Ethoxycarbonyl-1,1-difluoro-2-butyl methacrylate

https://huagongshe.com/reaction/1929271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
ReactantEthyl 2,2-difluoro-3-hydroxypentanoateHCID 59863825—
SolventWaterHCID 962—
Product1-Ethoxycarbonyl-1,1-difluoro-2-butyl methacrylateHCID 5986386166%

Reaction Conditions

Temperature55 °C

Reaction Steps

A 25 ml reactor was charged with 1.50 g (8.2 mmol) of ethyl 2,2-difluoro-3-hydroxypentanoate, 6.5 g of chloroform, 10 mg of an antioxidant NONFLEX MBP made by Seiko Chemical Co., Ltd., 1.03 g (9.9 mmol, 1.2 eq) of methacrylic chloride, and 1.25 g (12.4 mmol, 1.5 eq) of triethylamine, followed by stirring at 55° C. for 4 hours. Then, 10 g of water was added, followed by extraction with chloroform one time. The obtained organic layer was washed with diluted hydrochloric acid and water, followed by removing water with magnesium sulfate. After conducting filtration, chloroform was distilled off, thereby obtaining 2.06 g of the target 1-ethoxycarbonyl-1,1-difluoro-2-butyl methacrylate. Purity was 66%, and yield was 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08187787B2
Source datasetuspto-grants-2012_05
ORD IDord-edaaee7bd7544bc391c5648b672f0849
Source noteuspto-grants-2012_05