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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178790Generated: October 29, 2026

Triphenylmethyl phosphonium bromide → 1-[5-(Trifluoromethyl)-2-vinylphenyl]prop-2-en-1-ol

https://huagongshe.com/reaction/2178790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylmethyl phosphonium bromideHCID 21951224—
Reactant5-(Trifluoromethyl)-3-vinyl-1,3-dihydro-2-benzofuran-1-olHCID 59212646—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product1-[5-(Trifluoromethyl)-2-vinylphenyl]prop-2-en-1-olHCID 5921265682%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triphenylmethylphosphonium bromide (1.71 g, 4.78 mmol) was dissolved in ether (20.00 mL). After cooling to 0° C., a 1.60 M solution of n-butyllithium in hexane (2.72 mL) was added rapidly by syringe and the resulting orange mixture was warmed to room temperature and stirred overnight. The stirring was stopped to allow the solids to settle and then the yield was transferred via cannula to a solution of 5-(trifluoromethyl)-3-vinyl-1,3-dihydro-2-benzofuran-1-ol (1.00 g, 4.34 mmol) in ether (10.00 mL) while stirring at 0° C. Following the addition, the ice bath was removed and the mixture was heated to reflux overnight. The reaction was allowed to cool and then the solids filtered off and washed with a small amount of ether. Most of the solvents were evaporated and the crude product was loaded onto silica gel and eluted with hexane/EtOAc (10:1) to give the desired product (0.81 g, 82%), LC-MS [M+1]=229.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067921B2
Source datasetuspto-grants-2015_06
ORD IDord-39403f0cda52483b912afd5cf1631fc3
Source noteuspto-grants-2015_06