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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425477Generated: October 27, 2026

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

https://huagongshe.com/reaction/2425477

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 59127187—

Reaction Steps

Iodo-trimethyl-silane (CAS no. 16029-98-4) (115 mL, 0.79 mol) was added to a solution of methyl 3-hydroxy-5-[(2S)-1-methoxypropan-2-yl]oxy-benzoate (CAS no. 863504-77-2) (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 minutes. 10% w/v Aqueous sodium thiosulfate pentahydrate (100 mL) was added to the mixture and stirred for 20 minutes. 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 desired compound (16.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964725B2
Source datasetuspto-grants-2011_06
ORD IDord-eee19a38c4f343bea80ce8b71fffd811
Source noteuspto-grants-2011_06