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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171353Generated: October 26, 2026

Benzyl Alcohol → 3-Benzyloxy-5-(Trifluoromethyl)Pyridine

https://huagongshe.com/reaction/2171353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant3-Chloro-5-(trifluoromethyl)pyridineHCID 2736698—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-Benzyloxy-5-(Trifluoromethyl)PyridineHCID 21851825—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 3-chloro-5-(trifluoromethyl)pyridine (10.0 g, 55.1 mmol) in N,N-dimethylformamide (DMF) (150 mL) was added dropwise phenylmethanol (5.96 g, 55.1 mmol) under nitrogen at rt. The reaction mixture was stirred at 40° C. for 2 h, diluted with water (300 mL) and extracted with ethyl acetate (300 mL×3). Combined organic parts were washed with brine, dried over anhydrous Na2SO4 and concentrated. The crude product (100 g) was used into next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051325B2
Source datasetuspto-grants-2015_06
ORD IDord-241cedde8fd9463b8d309d113463fe99
Source noteuspto-grants-2015_06