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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950702Generated: October 30, 2026

4-Acetamidobenzaldehyde → 4-Acetaminobenzyl alcohol

https://huagongshe.com/reaction/1950702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AcetamidobenzaldehydeHCID 73942—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-Acetaminobenzyl alcoholHCID 152141—

Reaction Steps

To a solution of 4-acetamidobenzaldehyde (10 g, 61.3 mmol) in methanol (100 mL) was added sodium borohydride (800 mg) at room temperature in portions. The reaction mixture was stirred over night, and the progress of reaction checked by TLC using 4:1 hexanes:EtOAc as eluent. Absence of starting material indicated the completion of reduction and the reaction mixture was concentrated in a rotavap. The residue was partitioned between water (25 mL) and ethyl acetate (4×50 mL) and the organic layer was washed with brine (25 mL). The ethyl acetate layer was dried over anhydrous sodium sulfate and the removal of the solvent gave the alcohol as a pale yellow solid, which was dried under high vacuum. 8.6 g (85%); 1H NMR (DMSO-d6): δ 2.0 (s, 3H), 4.5 (d, 2H), 5.2 (t, 1H), 7.25 (d, 2H), 7.55 (d, 2H), 9.95 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404651B2
Source datasetuspto-grants-2013_03
ORD IDord-ee4640e661bb4dbbab0369a24b98e499
Source noteuspto-grants-2013_03