Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrabutylammonium Fluoride → beta-Methylenephenethyl alcohol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 반응물 | tert-Butyl-dimethyl-(2-phenyl-allyloxy)-silane | HCID 67155247 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | beta-Methylenephenethyl alcohol | HCID 80106 | 99.8% |
반응 단계
To a well stirred solution of tert-butyl-dimethyl-(2-phenyl-allyloxy)-silane (1.3 g, 5.23 mmol) in tetrahydrofuran (10 mL) is slowly added a solution of a 1 N tetrabutylammonium fluoride in tetrahydrofuran (10.5 mL, 10.5 mmol). The reaction is allowed to stir for 20 min, quenched by the addition of a saturated aqueous solution of ammonium chloride and extracted several times with ethyl acetate The organic layers are combined, washed with water, brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is purified via silica gel chromatography (10% ethyl acetate in hexanes) to yield 700 mg of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08841291B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-040cf4c5b67048c3a151c517cf90500a |
| 출처 메모 | uspto-grants-2014_09 |