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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073795Generated: October 30, 2026

Acetic Anhydride → 2-Methyl-6-acetamidobenzyl alcohol

https://huagongshe.com/reaction/2073795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
Reactant(2-Amino-6-methylphenyl)methanolHCID 15339417—
SolventDichloromethaneHCID 6344—
Product2-Methyl-6-acetamidobenzyl alcoholHCID 1436846464.6%

Reaction Steps

To a suspension of 2-amino-6-methylbenzyl alcohol (30 g) in methylene chloride (300 ml) was added dropwise acetic anhydride (22.3 g) at 5° to 10° C. After being stirred for 3 hours, the mixture was neutralized with sodium bicarbonate aqueous solution to give precipitates. To said mixture was added chloroform to dissolve said precipitates and then the organic layer was washed with water and sodium chloride aqueous solution, dried over magnesium sulfate and evaporated in vacuo. The resultant residue was suspended in diethyl ether and the precipitates were collected by filtration to give 2-methyl-6-acetamidobenzyl alcohol (25.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920129
Source datasetuspto-grants-1990_04
ORD IDord-a80899f975f149b7b0505acf426b856d
Source noteuspto-grants-1990_04