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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781167Generated: October 30, 2026

4-Phenoxybenzaldehyde → (4-Phenoxyphenyl)methanol

https://huagongshe.com/reaction/1781167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxybenzaldehydeHCID 66139—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4-Phenoxyphenyl)methanolHCID 82619598.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-phenoxybenzaldehyde (10.0 g, 50 mmol) and 10 mL dry THF was added dropwise to a 0° C. suspension of lithium aluminum hydride (2.1 g, 55.3 mmol) and 100 mL dry THF. The reaction mixture was stirred for 1 hour at 0° C., then was quenched successively with 2.1 mL H20, 2.1 mL 10% NaOH, and 6.3 mL H2O. The resultant slurry was stirred for 1.5 hours at room temperature, then was filtered through Celite® and the filtrate was evaporated under reduced pressure to afford the title compound (9.9 g) as a white solid. 1HNMR (300 MHz, CDCl3) δ 1.68 (t, 1H), 4.68 (d, 2H), 7.00 (m, 4H), 7.10 (t, 1H), 7.35 (m, 4H). MS (DCl/NH3) m/e 183 (M+1, -H2O)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631401
Source datasetuspto-grants-1997_05
ORD IDord-738e7cb49cf74664a77d5d70d96138ca
Source noteuspto-grants-1997_05