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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912045Generated: November 1, 2026

Propylene Oxide → 2-Chloro-α-methyl-6-(trifluoromethyl)benzeneethanol

https://huagongshe.com/reaction/912045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene OxideHCID 6378—
Reactant3-ChlorobenzotrifluorideHCID 7374—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Chloro-α-methyl-6-(trifluoromethyl)benzeneethanolHCID 57812398—

Reaction Steps

To a solution of 1-chloro-3-(trifluoromethyl)benzene (1.0 g, 5.5 mmol) in THF (10.0 mL) was added 2.5 M of n-BuLi in hexane (2.2 mL) at −78° C. and stirred for 1 h. Propylene oxide (370 mg, 6.4 mmol) was added to the reaction mixture at −78° C. and slowly warmed to rt. The reaction mixture was stirred for an additional 30 min. The reaction mixture was quenched with sat. aq. NH4Cl and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na2SO4, and the solvent was removed under reduced pressure to give a yellow oil. The material was purified by silica gel chromatography using Hexane/EtOAc (80:20) as eluent to yield the desired product as a yellow oil. 1H NMR (CDCl3, 400 MHz): δ=1.33 (d, J=6.1 Hz, 3H), 1.40 (d, J=6.3 Hz, 1H), 3.08-3.22 (m, 2H), 4.21-4.33 (m, 1H), 7.29-7.34 (m, 1H), 7.58-7.64 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022206B2
Source datasetuspto-grants-2011_09
ORD IDord-43f191c6cec74e208fc737dca5baffb1
Source noteuspto-grants-2011_09