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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182643Generated: November 3, 2026

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

https://huagongshe.com/reaction/1182643

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 300 mL reactor was charged with 18.0 g (98.4 mmol) of 2,2-difluoro-3-hydroxypentanoic acid ethyl ester, 78 g of chloroform, 120 mg of an antioxidant NONFLEX MBP (a product of Seiko Chemical Co., Ltd.), 12.4 g (118.8 mmol/1.2 equivalents) of methacrylic acid chloride, and 15.0 g (148.8 mmol/1.5 equivalents) of triethylamine, followed by stirring at 55° C. for 4 hours. Then, 120 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, conducting a filtration, and distilling chloroform out, thereby obtaining 24.7 g of the target methacrylic acid 1-ethoxycarbonyl-1,1-difluoro-2-butyl ester. Upon this, purity was 66%, and yield was 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08663903B2
Source datasetuspto-grants-2014_03
ORD IDord-02c45156ab084297b6e0ef17e1bf81ff
Source noteuspto-grants-2014_03