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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530749Generated: October 30, 2026

2,2,2-Trifluoroacetophenone → HCID 54173602, compound

https://huagongshe.com/reaction/1530749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroacetophenoneHCID 9905—
ReactantHCID 21274172HCID 21274172—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 54173602HCID 5417360271.9%

Reaction Steps

A solution of butyllithium in n-hexane (8.5 ml of 1.6 molar) was added, dropwise, at room temperature and under a nitrogen atmosphere over 10 minutes to [3-(3-phenoxyphenyl)propyl]-triphenylphophonium bromide (7.67 g; 13.75 mmol) in absolute tetrahydrofuran (40 ml). After stirring for 2 hours, α,α,α-trifluoroacetophenone (2.18 g; 12.5 mmol) dissolved in absolute tetrahydrofuran (10 ml) was added dropwise. After stirring for 3 hours at room temperature, the mixture was added to ice-water, extracted with ether and the extract dried over sodium sulphate and evaporated. After chromotography on silica gel using hexane-toluene, there was obtained 4-(3-phenoxyphenyl)-1-phenyl-1-trifluoromethyl-1-butene (3.31 g=71.9% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037087E1
Source datasetuspto-grants-2001_03
ORD IDord-5636a85cd2e54cbd980e77ce50a98f35
Source noteuspto-grants-2001_03