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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20524Generated: October 25, 2026

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

https://huagongshe.com/reaction/20524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium Thiosulfate PentahydrateHCID 61475—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantSodium BicarbonateHCID 516892—
Reactantmethyl 3-hydroxy-5-[(1S)-2-methoxy-1-methylethoxy]benzoateHCID 59127146—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Productmethyl 3-hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]benzoateHCID 5912718747%

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745475B2
Source datasetuspto-grants-2010_06
ORD IDord-c13cbd53a2484403be1275b169a3f48d
Source noteuspto-grants-2010_06