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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22602생성일: 2026년 10월 23일

4-Pyrrolidinopyridine → Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-

https://huagongshe.com/ko/reaction/22602

반응식

참여 물질

역할이름HCID투입량
반응물4-PyrrolidinopyridineHCID 75567—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물3-(Hydroxymethyl)benzaldehydeHCID 13131455—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-HCID 10883279—

반응 단계

To a solution of 3-hydroxymethylbenzaldehyde (step 1) (3 g) in methylene chloride (15 mL) and triethylamine (4.1 mL) was slowly added t-butylchlorodiphenyl silane (8 mL). Finally, a few mgs of 4-pyrrolidinopyridine was added as a catalyst. The reaction mixture was stirred overnight at room temperature (R.T.). The solution was quenched with 25% ammonium acetate and extracted with ethyl acetate, which was washed with brine (2×), dried over sodium sulfate, filtered and evaporated to dryness. Purification by flash chromatography, using 4% ethyl acetate in hexane afforded the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428171
출처 데이터셋uspto-grants-1995_06
ORD IDord-1cffddb7e50e4d50a76e4abb31db29ea
출처 메모uspto-grants-1995_06