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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905980Generated: October 30, 2026

1-(Trifluoromethyl)cyclopropane-1-carboxylic acid → 1-(Trifluoromethyl)cyclopropanemethanol

https://huagongshe.com/reaction/905980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Trifluoromethyl)cyclopropane-1-carboxylic acidHCID 2778306—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventTetrahydrofuranHCID 8028—
Product1-(Trifluoromethyl)cyclopropanemethanolHCID 5099066177%

Reaction Conditions

Temperature40 °C

Reaction Steps

50 mL of borane dimethylsulfide 2M in THF were added dropwise at RT via an addition funnel to a solution of 1-trifluormethyl-cyclopropanecarboxylic acid (10 g, 64.90 mmol) in 100 mL of THF. The resulting clear solution was stirred at 40° C. for 24 hours before being cooled to 0° C. and quenched by slow addition of aqueous saturated NH4Cl. The biphasic slurry was filtered through celite. The organic layer was separated, and the aqueous layer was back extracted twice with AcOEt. The combined organic layers were dried (Na2SO4), filtered, and evaporated to give 7 g of (1-trifluoromethyl-cyclopropyl)-methanol (77% yield). Used as in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012974B2
Source datasetuspto-grants-2011_09
ORD IDord-71db62423b974cf1b979e42b2a743845
Source noteuspto-grants-2011_09