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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840707Generated: October 31, 2026

Sodium Thiosulfate → HCID 23443884, compound

https://huagongshe.com/reaction/1840707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23443883HCID 23443883—
ReactantSodium HypochloriteHCID 23665760—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 23443884HCID 2344388477%

Reaction Steps

To the mixture consisting of 30 mmol (7.58 g) of 1-chloro-3-toluensulfonyloxy-2-propanol, 1.5 mmol (234 mg) of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO), 33 mmol (3.4 g) of sodium bromide, 90 mmol (7.50 g) of sodium hydrogencarbonate, 75 ml of ethyl acetate and 35 ml of water was added dropwise 47 mmol (32 g) of sodium hypochlorite aqueous solution (1.5 mmol/g) under cooling with ice. Temperature of the reaction system was about 4° C. and pH was about 8.5. After the dropping was completed, stirring was further continued for 30 minute. Thereto was added 20 ml of a 5% sodium thiosulfate aqueous solution and the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, and filtered off and concentrated under reduced pressure to obtain a crude product. It was purified with silica gel column to obtain 5.79 g of 1-chloro-3-toluensulfonyloxy-2-propanon. The yield was 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06682916B2
Source datasetuspto-grants-2004_01
ORD IDord-e5ec1fe5323245afbf967714af7509ec
Source noteuspto-grants-2004_01