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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358370생성일: 2026년 10월 25일

Triethylamine → 4(RS)-t-butyldimethylsilyloxy-2-(4-hydroxybutylthio)-2-cyclopentenone

https://huagongshe.com/reaction/358370

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물4-Sulfanylbutan-1-olHCID 548261—
반응물HCID 13362510HCID 13362510—
용매MethanolHCID 887—
생성물4(RS)-t-butyldimethylsilyloxy-2-(4-hydroxybutylthio)-2-cyclopentenoneHCID 2044880881%

반응 단계

2.80 g (12.2 mmoles) of 4(R)-t-butyldimethylsilyloxy-2,3-epoxycyclopentanone and 1.30 g (12.2 mmoles) of 4-mercaptobutan-1-ol were dissolved in 12 ml of methanol, and with stirring 1.87 ml (13.5 mmoles) of triethylamine was added. The stirring was continued for 30 minutes. Ten milliliters of a saturated aqueous solution of ammonium chloride was added, and the mixture was concentrated. The residue was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated. The resulting oily product was chromatographed on a silica gel column using hexane/ethyl acetate (8/1) as an eluent to give 3.12 g (81%) of 4(RS)-t-butyldimethylsilyloxy-2-(4-hydroxybutylthio)-2-cyclopentenone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04466980
출처 데이터셋uspto-grants-1984_08
ORD IDord-50b7a521cf9c4e52b702724c63423584
출처 메모uspto-grants-1984_08