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HRID 342047生成日期:2026年10月23日

海萝胶 → 1-[(RS)-1-Cyano-[(S)-1-phenylpropylamino]methyl]-1-ethoxycarbonylcyclopropane

https://huagongshe.com/zh-CN/reaction/342047

反应方程式

参与物

角色名称HCID投料
反应物海萝胶HCID 313—
反应物氰化钾HCID 9032—
反应物(S)-(-)-1-苯丙胺HCID 6993773—
反应物1-甲酰基环丙烷-1-甲酸乙酯HCID 9964122—
溶剂乙醇HCID 702—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
产物1-[(RS)-1-Cyano-[(S)-1-phenylpropylamino]methyl]-1-ethoxycarbonylcyclopropaneHCID 7021120959.1%

反应步骤

An eggplant type flask was charged with 136 mg of potassium cyanide, 501 mg of (S)-1-phenylpropylamine and 1 ml of water. After adding 152 mg of ethyl 1-formylcyclopropane-1-carboxylate dissolved in 2 ml of ethanol, dropwise at room temperature, the resulting mixture was further mixed with 0.2 ml of concentrated hydrochloric acid, and stirred for 1 hour at the same temperature and then for 2 hours at 50° C. After confirming completion of the reaction, the reaction solution was mixed with ice water and extracted with ethyl acetate. Next, the resulting organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate and, after removing insoluble matter by filtration, the solvent was evaporated under a reduced pressure. Thereafter, the resulting residue was subjected to a silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain 181 mg (59%) of a diastereomer mixture in the form of colorless oil. Formation ratio of the two diastereomers was calculated under the following analytical conditions.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05856518
来源数据集uspto-grants-1999_01
ORD IDord-d5a95cc5e12c49ebb314619c0387ebd4
来源说明uspto-grants-1999_01