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HRID 20524作成日:2026年10月25日

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

https://huagongshe.com/reaction/20524

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium Thiosulfate PentahydrateHCID 61475—
反応物Trimethylsilyl iodideHCID 85247—
反応物Sodium BicarbonateHCID 516892—
反応物methyl 3-hydroxy-5-[(1S)-2-methoxy-1-methylethoxy]benzoateHCID 59127146—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
生成物methyl 3-hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]benzoateHCID 5912718747%

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745475B2
出典データセットuspto-grants-2010_06
ORD IDord-c13cbd53a2484403be1275b169a3f48d
出典メモuspto-grants-2010_06