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HRID 246891作成日:2026年10月26日

Acetone → (S)-1,2-Bis(N-Isopropylamino)-3-Phenylpropane

https://huagongshe.com/reaction/246891

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Calcium SulfateHCID 24497—
反応物Sodium borohydrideHCID 4311764—
反応物(2S)-3-Phenylpropane-1,2-diamineHCID 12699301—
溶媒BenzeneHCID 241—
溶媒MethanolHCID 887—
生成物(S)-1,2-Bis(N-Isopropylamino)-3-PhenylpropaneHCID 13689690—

反応条件

温度-10 °C

反応手順

21.2 mmoles (3.18 grams) of (S)-1,2-diamino-3-phenylpropane were dissolved in 12 ml of benzene, treated with 42.4 mmoles (3.11 ml) of acetone and a spatula tip of p-toluenesulfonic acid. The mixture was heated for 12 hours under reflux in a Soxhlet apparatus which is filled with calcined calcium sulfate as drying agent. After drawing off the solvent in a vacuum there was obtained a light yellowish oil. It was dissolved in 50 ml of methanol, cooled in an ice-salt bath to -10° C. and treated with 80.0 mmoles (3.03 grams) of NaBH4. It was allowed to come to room temperature under stirring and heated for a further 12 hours under reflux. After cooling the solvent was distilled in a vacuum and hydrolyzed with 30 ml of water. It was shaken with 150 ml of ether and the organic phase washed twice with 30 ml of water each time. After drying over sodium sulfate the ether was drawn off and the brownish oil obtained was distilled in a high vacuum at 100° C. air bath temperature. Colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04704464
出典データセットuspto-grants-1987_11
ORD IDord-71e66b841793402f9f6887b36d7d0fef
出典メモuspto-grants-1987_11