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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666422Generated: October 31, 2026

3-Hydroxybenzyl alcohol → (3-(4-(Trifluoromethyl)phenoxy)phenyl)methanol

https://huagongshe.com/reaction/1666422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzyl alcoholHCID 102—
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 1-fluoro-4-(trifluoromethyl)-HCID 67873—
SolventDimethyl SulfoxideHCID 679—
Product(3-(4-(Trifluoromethyl)phenoxy)phenyl)methanolHCID 2313640760.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

3-Hydroxymethyl-phenol (1.0 g, 8.1 mmol), 4-fluorobenzotrifluoride (1.32 g, 8.1 mmol) and cesium carbonate (3.28 g, 10.1 mmol) were suspended in dimethylsulfoxide (15 mL) and heated to 110° C. After stirring for 16 h, the reaction was partitioned between water (150 mL) and ethyl acetate (150 mL). The organic layer was separated and the aqueous was extracted again with ethyl acetate. The combined organic layer was dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (10-40%, EtOAc:heptane) to afford the title compound (1.32 g) as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-8b018529f8d64f4faf6f6d7669e52933
Source noteuspto-grants-2011_10