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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710883Generated: October 30, 2026

Acetic Anhydride → 3-Acetaminobenzyl alcohol

https://huagongshe.com/reaction/1710883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant3-Aminobenzyl alcoholHCID 80293—
SolventTetrahydrofuranHCID 8028—
Product3-Acetaminobenzyl alcoholHCID 9663974.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (3-aminophenyl)methanol (1.87 g, 14.7 mmol) in tetrahydrofuran (10 mL) was added triethylamine (7 mL, 73.5 mmol). The reaction was cooled down to 0° C., acetic anhydride (1.5 mL, 16 mmol) was added dropwise. The reaction was warmed to room temperature overnight. The reaction mixture was partitioned between ethyl acetate and H2O. The ethyl acetate layer was dried over MgSO4, concentrated, trituated with CH2Cl2 to yield N-(3-(hydroxymethyl)phenyl)acetamide as a yellow solid (1.8 g, 74%). HPLC retention time (Method C)=1.03 min. LC/MS (ESI) (M+H)+=166.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790745B2
Source datasetuspto-grants-2010_09
ORD IDord-acf3aa17ed994537a2900057ae80fb57
Source noteuspto-grants-2010_09