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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425764Generated: November 2, 2026

Sodium Thiosulfate → HCID 59822462, compound

https://huagongshe.com/reaction/2425764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22965782HCID 22965782—
SolventDichloromethaneHCID 6344—
ProductHCID 59822462HCID 5982246259%

Reaction Steps

A mixture of 4-ethylidenetetrahydro-2H-pyran (about 500 mg, step 1) and 3-chloroperoxybenzoic acid (1.11 g, 4.49 mmol) in dichloromethane (50 mL) was stirred at 0° C. to room temperature for 1 h. Then, saturated aqueous sodium hydrogen carbonate solution (50 mL) and saturated aqueous sodium thiosulfate solution (50 mL) were added, and the aqueous layer was extracted with dichloromethane (100 mL×3). The combined organic layer was dried over magnesium sulfate, and concentrated in vacuo to give 337 mg of the crude title compound as a yellow oil. This was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964727B2
Source datasetuspto-grants-2011_06
ORD IDord-ca42f55ad8a149e0a7106ab7cd3e55c1
Source noteuspto-grants-2011_06