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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Benzyloxy-3-chloro-2-propanolHCID 4141006—
ReactantSodium HypochloriteHCID 23665760—
Catalyst4-Acetamido-TEMPOHCID 518988—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(Benzyloxy)-3-chloropropan-2-oneHCID 1118323367.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06682916B2
Source datasetuspto-grants-2004_01
ORD IDord-38f06e56a4f849e2959032ea787ae214
Source noteuspto-grants-2004_01