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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216352Generated: October 25, 2026

Methyl trifluoromethyl ketone → Benzyl 4,4,4-trifluoro-3-methylbut-2-enoate

https://huagongshe.com/reaction/216352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl trifluoromethyl ketoneHCID 9871—
ReactantBenzyl 2-(triphenyl-lambda5-phosphanylidene)acetateHCID 3862746—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4,4,4-trifluoro-3-methylbut-2-enoateHCID 66705445—

Reaction Steps

1,1,1-Trifluoroacetone (680 mg, 6.1 mmol) was added to an ambient temperature solution of benzyl (triphenylphosphoranylidene)acetate (2.5 g, 6.1 mmol) in methylene chloride (10 mL). After stirring in a sealed tube for 72 h, the reaction mixture was concentrated in vacuo. Chromatography over silica eluting with 0-20% ethyl acetate/hexane afforded benzyl 4,4,4-trifluoro-3-methylbut-2-enoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193228B2
Source datasetuspto-grants-2012_06
ORD IDord-787f6bbc5f2b4757878113bd726cbc64
Source noteuspto-grants-2012_06