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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20524생성일: 2026년 10월 24일

Sodium Thiosulfate Pentahydrate → methyl 3-hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]benzoate

https://huagongshe.com/ko/reaction/20524

반응식

참여 물질

역할이름HCID투입량
반응물Sodium Thiosulfate PentahydrateHCID 61475—
반응물Trimethylsilyl iodideHCID 85247—
반응물Sodium BicarbonateHCID 516892—
반응물methyl 3-hydroxy-5-[(1S)-2-methoxy-1-methylethoxy]benzoateHCID 59127146—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물methyl 3-hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]benzoateHCID 5912718747%

반응 단계

Trimethylsilyl iodide (115 mL, 0.79 mol) was added to a solution of methyl 3-hydroxy-5-[(1S)-2-methoxy-(1-methylethyl)oxy]benzoate (38.01 g, 0.158 mol) in acetonitrile (500 mL) and stirred for 24 hours. Methanol (300 mL) was added and the reaction stirred for 10 mins. 10% w/v Aqueous sodium thiosulfate pentahydrate (100 mL) was added to the mixture and stirred for 20 mins. The reaction mixture was neutralised with saturated aqueous sodium bicarbonate solution, the organic solvents removed in vacuo, and the product extracted into ethyl acetate (4×100 mL). The combined organic layers were dried (MgSO4), filtered and the solvents removed in vacuo. The crude material was crystallised from ethyl acetate to give the title compound (16.80 g)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745475B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c13cbd53a2484403be1275b169a3f48d
출처 메모uspto-grants-2010_06