참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl 3-(p-tert-butylphenoxy)-propionate | HCID 14423333 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 3-p-t-Butyl-phenoxypropanol | HCID 13313735 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05242936 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-5c7452413c6c4954b4611120e361a41f |
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| 출처 메모 | uspto-grants-1993_09 |
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