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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361621Generated: October 28, 2026

4-Acetamidobenzaldehyde → 4-Acetaminobenzyl alcohol

https://huagongshe.com/reaction/2361621

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691787B2
Source datasetuspto-grants-2014_04
ORD IDord-ed173927ef5a4e5db8575b7c022bc0cb
Source noteuspto-grants-2014_04