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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750530Generated: October 26, 2026

Methanol → (5-(Trifluoromethyl)pyridin-2-yl)methanol

https://huagongshe.com/reaction/1750530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Iodo-5-(trifluoromethyl)pyridineHCID 22147841—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product(5-(Trifluoromethyl)pyridin-2-yl)methanolHCID 3820787—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To the solution of 2-iodo-5-(trifluoromethyl)pyridine (CAS number 100366-75-4; 10 g, 69.4 mmol) in toluene (250 ml) at −78° C. was added n-BuLi in hexane (2.5 M, 15.0 mL, 37.5 mmol). The reaction was stirred at −78° C. for 15 minutes. To this was then added drop wise DMF (3.5 ml) and then stirred at −78° C. for 1 hour. Sodium borohydride (2.74 g, 72.0 mmol) and methanol (50 ml) were added and the resulting reaction mixture was stirred for 30 minutes and then allowed to warm to room temperature. The reaction was cooled to −10° C. and to this was then added a saturated solution of ammonium chloride. The organics were extracted with ethyl acetate (2×200 ml) and the combined organics were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156829B2
Source datasetuspto-grants-2015_10
ORD IDord-8996f018033549598783e35e5a0c1197
Source noteuspto-grants-2015_10