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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77326생성일: 2026년 10월 24일

Tetrabutylammonium Fluoride → beta-Methylenephenethyl alcohol

https://huagongshe.com/ko/reaction/77326

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물tert-Butyl-dimethyl-(2-phenyl-allyloxy)-silaneHCID 67155247—
용매TetrahydrofuranHCID 8028—
생성물beta-Methylenephenethyl alcoholHCID 8010699.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841291B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-040cf4c5b67048c3a151c517cf90500a
출처 메모uspto-grants-2014_09