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HRID 10349作成日:2026年10月26日

Ethyl Acetate → 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/10349

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Ammonium HydroxideHCID 14923—
反応物Benzyl 2-methyl-1-oxa-5-azaspiro[2.4]heptane-5-carboxylateHCID 21041146—
溶媒MethanolHCID 887—
生成物3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl esterHCID 69068640—

反応手順

A solution of 2-methyl-1-oxa-5-azaspiro[2,4]heptane-5-carboxylic acid benzyl ester (Example A9, 0.31 g, 1.25 mmol) in methanol (10 mL) and ammonium hydroxide (7 mL) is heated in a sealed tube at 100° C. for 16 hours. After cooling, the reaction mixture is dissolved ethyl acetate, washed with water, dried over Na2SO4 and evaporated to afford the title compound (0.340 g). 1H NMR (200 MHz, CDCl3): δ 7.33–7.26 (m, 5H), 5.28 (bs, 2H), 5.07 (s, 2H), 3.56–3.16 (m, 5H), 2.03–1.76 (m, 2H), 1.15 (d, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094780B1
出典データセットuspto-grants-2006_08
ORD IDord-25d841ff62cf41b6862babb19ab9536f
出典メモuspto-grants-2006_08