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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371559Generated: November 2, 2026

Methanol → Methyl 3-aminophenylacetate

https://huagongshe.com/reaction/1371559

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 numberUS07157476B2
Source datasetuspto-grants-2007_01
ORD IDord-a68855b8c9a545ddb1818a67ec74226b
Source noteuspto-grants-2007_01