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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643886Generated: October 30, 2026

Allyl bromide → 1,1,1-trifluoro-4-penten-2-ol

https://huagongshe.com/reaction/643886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthanol, 1-ethoxy-2,2,2-trifluoro-HCID 9897—
ReactantIndiumHCID 5359967—
SolventWaterHCID 962—
Product1,1,1-trifluoro-4-penten-2-olHCID 10909642—

Reaction Steps

To a suspension of indium powder (2.3 g, 20 mmol) in water is added allyl bromide (2.5 mL, 30 mmol) followed by trifluoroacetaldehyde ethyl hemiacetal (1.3 mL, 10 mmol). The reaction mixture is stirred for 16 h and then extracted with t-butyl methyl ether (50 mL). The organic layer is washed with water, brine, dried with Na2SO4 and concentrated to give the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700633B2
Source datasetuspto-grants-2010_04
ORD IDord-636cfc354b1d4693a020b3939d191a51
Source noteuspto-grants-2010_04