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HRID 1493369作成日:2026年10月26日

Butyl 3-(p-tert-butylphenoxy)-propionate → 3-p-t-Butyl-phenoxypropanol

https://huagongshe.com/reaction/1493369

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl 3-(p-tert-butylphenoxy)-propionateHCID 14423333—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒Diethyl EtherHCID 3283—
生成物3-p-t-Butyl-phenoxypropanolHCID 13313735—

反応条件

温度-5 °C

反応手順

This ester 21.0 g was dissolved in 500 ml dry ether and cooled to -5° C. in an ice/acetone bath. To the cold solution was added, cautiously, a slurry of 3.5 g lithium aluminum hydride in 100 ml dry ether. After one hour the excess lithium aluminum hydride was destroyed by the cautious addition of 200 ml ethyl acetate, then 50 ml water. The solution was filtered and the filtrate partitioned between 200 ml ether-200 ml water. The organic layer was removed, dried, and evaporated to a yellow oil which was vacuum distilled (116° C./0.35 mm) over potassium carbonate to a clear colorless oil, 3-p-t-butylphenoxypropanol, 10.1 g (64%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05021460
出典データセットuspto-grants-1991_06
ORD IDord-886c7ec6d20f4b46b4e5b33dc34860ab
出典メモuspto-grants-1991_06