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HRID 224556作成日:2026年10月26日

Ethyl Acetate → (4S)-Oct-1-yn-4-ol

https://huagongshe.com/reaction/224556

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Potassium HydroxideHCID 14797—
反応物1-Octyn-4-olHCID 103656—
反応物HCID 53798844HCID 53798844—
溶媒Methanol--water (1/1)HCID 22242641—
生成物(4S)-Oct-1-yn-4-olHCID 12786164—

反応手順

A solution of 1.15 g (5.0 mmoles) of (S)-4-benzoyloxy-1-octyne (Example 19) and 1.40 g (25 mmoles) of potassium hydroxide in 50 ml of 10:1 methanol-water is allowed to stand at toom temperature for 24 hours. The bulk of the methanol is evaporated at room temperature, and the mixture is extracted with ether. The extract is washed with brine, dried over magnesium sulfate, and evaporated to give a colorless oil, identical to 4-hydroxy-1-octyne [α]D25 =+17°±1.0° (C=0.77, ethyl acetate). This compound has the (S)-configuration.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04233231
出典データセットuspto-grants-1980_11
ORD IDord-9f7b0008348d45d9a9310187f22895d8
出典メモuspto-grants-1980_11