HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840705Generated: October 25, 2026
Sodium Thiosulfate → 1-(Benzyloxy)-3-chloropropan-2-one
https://huagongshe.com/reaction/1840705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Benzyloxy-3-chloro-2-propanol | HCID 4141006 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | 4-Acetamido-TEMPO | HCID 518988 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(Benzyloxy)-3-chloropropan-2-one | HCID 11183233 | 67.1% |
Reaction Steps
To the mixture consisting of 30 mmol (6.0 g) of 1-benzyloxy-3-chloro-2-propanol, 1.5 mmol (320 mg) of 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxyl, 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 sodium sulfate, filtered off and concentrated under reduced pressure to obtain a crude product. It was purified with silica gel column to obtain 4 g of 1-chloro-3-benzyloxy-2-propanon. The yield was 67%.
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-38f06e56a4f849e2959032ea787ae214 |
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| Source note | uspto-grants-2004_01 |
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