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HRID 16215생성일: 2026년 10월 25일

2-Butene-1,4-diol → 4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol

https://huagongshe.com/reaction/16215

반응식

참여 물질

역할이름HCID투입량
반응물2-Butene-1,4-diolHCID 8065—
반응물Sodium hydrideHCID 24758—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
용매TetrahydrofuranHCID 8028—
생성물4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-olHCID 66656949—

반응 단계

NaH (3 g, 75 mmol, 60% in oil) was added portion-wise to a stirred and cooled (0° C.) solution of but-2-ene-1,4-diol (6 g, 68.09 mmol) in dry tetrahydrofuran (250 mL). After the addition, the mixture was allowed to warm to room temperature and stirred for another two hours. The resulting white mixture was then cooled (0° C.) and tert-butyl-chlorodiphenylsilane (15.7 mL, 61.28 mmol) was added drop wise. After twenty minutes, the cooling bath was removed and the mixture was allowed to stir overnight at room temperature. Saturated NH4Cl was poured into the reaction mixture and the reaction was partitioned with diethyl ether (200 mL). The organic layer was washed with brine, dried (MgSO4), and filtered. The resulting oil was used in the following step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737137B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-cacae96a195b4eb7a82169604af3d677
출처 메모uspto-grants-2010_06