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HRID 5007作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/5007

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 filtrated 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US05242936
出典データセットuspto-grants-1993_09
ORD IDord-5c7452413c6c4954b4611120e361a41f
出典メモuspto-grants-1993_09