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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445337생성일: 2026년 10월 25일

Chlorotrimethylsilane → (4,5-Diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetate

https://huagongshe.com/reaction/1445337

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(4,5-Diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzoyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetateHCID 21045301—
용매AcetonitrileHCID 6342—
생성물(4,5-Diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetateHCID 21045302—

반응 조건

온도0 °C

반응 단계

630 mg of (4,5-diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzoyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetate were dissolved in 30 ml of acetonitrile and cooled to 0° C. in an ice bath. 1.31 ml of trimethylchlorosilane and 652 mg of sodium cyanoborohydride were added, the ice bath was removed and the reaction was stirred for 2 h. 100 ml of water were added to the reaction mixture, which was extracted twice with 70 ml of dichloromethane each time. The combined organic phases were washed with 50 ml of saturated sodium chloride solution, dried over sodium sulfate and concentrated. The crude product was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666848B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-f73d86f60a234e4c8299a158556fc0b4
출처 메모uspto-grants-2010_02