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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384144Generated: October 29, 2026

Water → 2-(2-Phenoxyphenyl)ethanol

https://huagongshe.com/reaction/384144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactanto-PhenoxybenzaldehydeHCID 88060—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventDiiodomethaneHCID 6346—
SolventHCID 178418348HCID 178418348—
Product2-(2-Phenoxyphenyl)ethanolHCID 19849143—

Reaction Steps

To a solution of 2-phenoxybenzaldehyde (535 mg) in tetrahydrofuran (5 ml), 0.326 ml of diiodomethane and 5.4 ml of methyllithium (1.0M diethyl ether solution) were added under ice-cooling, and the reaction solution was stirred at the same temperature for 30 minutes and then at room temperature for 1 hour. To the reaction solution was added water, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to afford a crude product as a yellow oil. To a solution of the crude product in tetrahydrofuran (5 ml), 284 mg of sodium cyanoborohydride and 0.569 ml of trifluoroborane-diethyl ether complex were added under ice-cooling, and the reaction solution was stirred at the same temperature for 50 minutes. To the reaction solution was added a saturated saline solution, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (95:5-50/50)) to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367708B2
Source datasetuspto-grants-2013_02
ORD IDord-51b92cf373b441cab84b850b9e07ca68
Source noteuspto-grants-2013_02