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HRID 342046作成日:2026年10月26日

Potassium Cyanide → 1-[(RS)-1-Cyano-[(S)-1-(1-naphthyl)ethylamino]methyl]-1-ethoxycarbonylcyclopropane

https://huagongshe.com/reaction/342046

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CyanideHCID 9032—
反応物1-Naphthalenemethanamine, alpha-methyl-, (alphaS)-HCID 66325—
反応物Ethyl 1-formylcyclopropanecarboxylateHCID 9964122—
反応物Sodium BisulfiteHCID 23665763—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1-[(RS)-1-Cyano-[(S)-1-(1-naphthyl)ethylamino]methyl]-1-ethoxycarbonylcyclopropaneHCID 1539105472.2%

反応条件

温度50 °C

反応手順

An eggplant type flask was charged with 426 mg of ethyl 1-formylcyclopropane-1-carboxylate to which were further added 771 mg of (S)-1-(1-naphthyl)ethylamine dissolved in 5 ml of ethanol, 293 mg of potassium cyanide dissolved in 2 ml of water and 937 mg of sodium hydrogen sulfite in that order at 0° C. The reaction system was stirred for 3.5 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=5:1) to obtain 698 mg (72%) of a diastereomer mixture in the form of colorless oil. Formation ratio of the two diastereomers was calculated under the following analytical conditions.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05856518
出典データセットuspto-grants-1999_01
ORD IDord-8a5d6db9e9b14ad998ba0ad650c1591d
出典メモuspto-grants-1999_01