HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840707Generated: October 31, 2026
Sodium Thiosulfate → HCID 23443884, compound
https://huagongshe.com/reaction/1840707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 23443883 | HCID 23443883 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | Tempo | HCID 2724126 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23443884 | HCID 23443884 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06682916B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-e5ec1fe5323245afbf967714af7509ec |
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| Source note | uspto-grants-2004_01 |
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