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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39256Generated: October 26, 2026

4-Hydroxybenzyl Alcohol → 4-Acetoxybenzyl alcohol

https://huagongshe.com/reaction/39256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Product4-Acetoxybenzyl alcoholHCID 9590629%

Reaction Steps

To a solution of 4-hydroxybenzyl alcohol (7.5 g, 60 mmol) and 8.4 mL of triethylamine (8.4 mL, 60 mmol) in 100 mL of ethyl acetate, cooled in an ice bath, was added, via canula over 15 min, a solution of acetyl chloride (4.7 mL, 66 mmol) in 50 mL of ethyl acetate. The mixture was stirred in the same bath, which was left to come to room temperature on its own. After 18 h, the precipitate was removed by filtration. It was rinsed with 50 mL of ethyl acetate in small portions. The combined filtrates were concentrated in vacuo and purified by flash chromatography on silica gel, using 3:2 hexanes:ethyl acetate as the eluent, to afford 60 (2.853 g, 17 mmol, 29%) as an oil. 1H NMR (400 MHz, CDCl3) δ 2.31 (s, 3H), 4.69 (d, J=5.8 Hz, 2H), 7.08 (d, J=8.6 Hz, 2H), 7.38 (d, J=8.4 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524691B2
Source datasetuspto-grants-2013_09
ORD IDord-0b23a32192a74823a75b3149f61fe6ce
Source noteuspto-grants-2013_09