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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957335Generated: November 2, 2026

4-Phenoxybenzaldehyde → (4-Phenoxyphenyl)methanol

https://huagongshe.com/reaction/1957335

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 H2O, 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. 1H NMR (300 MHz, CDCl3) δ1.68 (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 numberUS05783593
Source datasetuspto-grants-1998_07
ORD IDord-b428dc93b9f84669a5fd88ef51209104
Source noteuspto-grants-1998_07