Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411782Generated: October 31, 2026

Acetyl chloride → 4-(Acetoxymethyl)benzoic acid

https://huagongshe.com/reaction/411782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Product4-(Acetoxymethyl)benzoic acidHCID 7021590—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (15.4 ml, 110.4 mmol) was added to a solution of aldehyde (2) (12.57 g, 92.4 mmol) in THF (50 ml) and cooled to 0° C. Acetyl chloride (7.91 g, 110.4 mmol) was then gradually added over 25 minutes, and the mixture was then left to stir for two hours at room temperature. After one hour, ethyl acetate (200 ml) was added and the solution washed with sodium carbonate (100 ml), HCl (17%, 50 ml) and water (100 ml) respectively. The organic layer was then dried over sodium sulfate and the solvent removed under reduced pressure to give an oil which crystallised when cooled. Re-crystallisation in methanol-hexane gave light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559256B2
Source datasetuspto-grants-2003_05
ORD IDord-bd2bf2d02ab64519a5da2a2809b8859d
Source noteuspto-grants-2003_05