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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5007생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Butyl 3-(p-tert-butylphenoxy)-propionateHCID 14423333—
반응물Aluminium lithium hydrideHCID 21226445—
용매Diethyl EtherHCID 3283—
생성물3-p-t-Butyl-phenoxypropanolHCID 13313735—

반응 조건

온도-5 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242936
출처 데이터셋uspto-grants-1993_09
ORD IDord-5c7452413c6c4954b4611120e361a41f
출처 메모uspto-grants-1993_09