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HRID 491536作成日:2026年10月27日

Methanol → Methyl 3-aminophenylacetate

https://huagongshe.com/reaction/491536

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Thionyl ChlorideHCID 24386—
反応物(3-Aminophenyl)acetic acidHCID 571807—
生成物Methyl 3-aminophenylacetateHCID 13054266—

反応条件

温度0 °C

反応手順

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 while 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) to afford methyl 3-aminophenylacetate as a brown oil. (14.1 g, 83%). 1H NMR (CDCl3) δ 7.12 (1H, dd), 6.7-6.6 (3H, m), 3.71 (3H, s), 3.55 (2H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531556B2
出典データセットuspto-grants-2009_05
ORD IDord-5490efe37fbc4a6b8c5795ef65309bf1
出典メモuspto-grants-2009_05