Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412548Generated: November 1, 2026

Sodium Thiosulfate → 4-(1-Tert-butoxycarbonylpyrrolidin-3-yloxy)phenol

https://huagongshe.com/reaction/412548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(1-tert-Butoxycarbonylpyrrolidin-3-yloxy)benzaldehydeHCID 18536505—
SolventDichloromethaneHCID 6344—
Product4-(1-Tert-butoxycarbonylpyrrolidin-3-yloxy)phenolHCID 1853636873%

Reaction Steps

To a solution of 4-(1-tert-butoxycarbonylpyrrolidin-3-yloxy)benzaldehyde (500 mg) in methylene chloride (10 ml) was added 70% 3-chloroperbenzoic acid (712 mg) with ice-cooling, and the mixture was stirred at room temperature for 4.5 hours. After completion of the reaction, aqueous sodium hydrogencarbonate solution and aqueous sodium thiosulfate solution were added, and the mixture was extracted with methylene chloride and washed successively with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated. The obtained residue was dissolved in methanol (3.4 ml) and thereto was added 1N aqueous sodium hydroxide solution (1.7 ml), and the mixture was stirred at room temperature for 1 hour. After completion of the reaction, 10% aqueous citric acid solution was added, and the mixture was extracted with chloroform and washed successively with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated. The obtained solid was washed with diethyl ether and dried under reduced pressure to give the title compound (350 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562828B1
Source datasetuspto-grants-2003_05
ORD IDord-47e83552dc44454a8eebfe95d7564c83
Source noteuspto-grants-2003_05