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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108722Generated: October 30, 2026

Methanol → Methyl 3-aminophenylacetate

https://huagongshe.com/reaction/2108722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant(3-Aminophenyl)acetic acidHCID 571807—
ProductMethyl 3-aminophenylacetateHCID 13054266—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Aminophenylacetic acid (15.5 g, 0.10 mol) was suspended in methanol (150 mL) and cooled to 0° C. Thionyl chloride (11.2 mL, 0.15 mol) was added dropwise under stirring. A clear orange solution was obtained, which was stirred for 4 hours, then evaporated. The solid residue was partitioned between ethyl acetate (150 mL) and saturated sodium bicarbonate (150 mL) and the organic phase washed with saturated sodium bicarbonate (100 mL), and brine and dried (Na2SO4). Methyl 3-aminophenylacetate was isolated as a brown oil. (14.1 g, 83%). 1H NMR (500 MHz, CDCl3) δ 7.12 (1H, dd), 6.7-6.6 (3H, m), 3.71 (3H, s), 3.55 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514448B2
Source datasetuspto-grants-2009_04
ORD IDord-67ea454c6d6b4d47a8ede6a4fcd9ccc3
Source noteuspto-grants-2009_04