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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534839Generated: October 29, 2026

Hydride → (3-Chloro-5-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/534839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrideHCID 166653—
ReactantMethyl 3-chloro-5-(trifluoromethyl)benzoateHCID 46311109—
SolventTetrahydrofuranHCID 8028—
Product(3-Chloro-5-(trifluoromethyl)phenyl)methanolHCID 3857254102%

Reaction Steps

To a stirred solution of methyl 3-chloro-5-(trifluoromethyl)benzoate (Reference Example 29, 2.20 g, 9.22 mmol) in THF (100.0 mL) at −78° C. was added disobutylaluminum hydride solution (28.00 mL, 1.0 M in methylene chloride, 28.00 mmol) and the resulting reaction mixture was stirred at this temperature for 4 h. After this time, the reaction was quenched with 1.0 M hydrochloric acid (100 mL) and warmed to room temperature. The reaction mixture was diluted with ethyl acetate, washed with aqueous 1.0 M hydrochloric acid, water, and saturated sodium chloride, dried (Na2SO4), filtered, concentrated under reduced pressure to provide (3-chloro-5-(trifluoromethyl)phenyl)methanol (1.98 g, >99%) as a brown oil, which was used without further purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-cb78efaa19254d6baa7b88449fb720a0
Source noteuspto-grants-2014_10