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HRID 1432413作成日:2026年10月24日

Benzyl chloroformate → 4-(((Benzyloxy)(hydroxy)methylidene)amino)cyclohexane-1-carboxylic acid

https://huagongshe.com/ja/reaction/1432413

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl chloroformateHCID 10387—
反応物4-Aminocyclohexanecarboxylic acidHCID 171560—
反応物Sodium BicarbonateHCID 516892—
溶媒1,4-DioxaneHCID 31275—
生成物4-(((Benzyloxy)(hydroxy)methylidene)amino)cyclohexane-1-carboxylic acidHCID 28524759.2%

反応条件

温度0 °C

反応手順

Benzyl chloroformate (2.2 mL, 15.4 mmol) was added to a solution of 4-amino-cyclohexanecarboxylic acid (2 g, 14.0 mmol) in a mixture of 1,4-dioxane (5 mL) and saturated sodium bicarbonate aqueous solution (5 mL). The mixture was stirred at 0° C. for 3 hours. Dioxane was removed under reduced pressure. The residue was partitioned between ethyl acetate and water. The ethyl acetate solution was washed with brine, dried over sodium sulfate, filtered, and concentrated to give 2.3 g (59%) of 4-benzyloxycarbonylamino-cyclohexanecarboxylic acid as yellow oil. MS (ESP−) m/z 276.39 (M−1). 1H NMR (300 MHz, CDCl3) δ 7.34 (m, 5H), 5.09 (s, 2H), 2.24 (m, 1H), 2.04 (m, 2H), 1.83 (m, 2H), 1.44 (m, 3H), 0.97 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612094B2
出典データセットuspto-grants-2009_11
ORD IDord-6c69283da5d7425f8e8e14bb48941e17
出典メモuspto-grants-2009_11