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HRID 1044621作成日:2026年10月24日

Water → (1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylic acid

https://huagongshe.com/ja/reaction/1044621

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylateHCID 59833587—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylic acidHCID 5983354863.4%

反応条件

温度80 °C

反応手順

To a stirred solution of methyl (1S,4S)-4-[(tert-butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate (0.78 g, 2.6 mmol) in tetrahydrofuran (1.5 mL), methanol (15 mL), and water (3.0 mL) was added lithium hydroxide monohydrate (0.55 g, 13 mmol) and the resulting orange mixture was stirred at 80° C. overnight. The solvents were evaporated and the mixture was acidified with 6 N HCl to a pH of about 4. The aqueous was then extracted with methylene chloride three times. The combined organic layers were dried (MgSO4), filtered, and concentrated in vacuo to give the desired product as an oil (0.47 g, 63.2%). LCMS calculated for C14H24NO5: (M+H) 286.2; found 286.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563582B2
出典データセットuspto-grants-2013_10
ORD IDord-4c37e3b4be184998913a9b68fa469032
出典メモuspto-grants-2013_10