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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368045Generated: October 30, 2026

Sodium Thiosulfate → HCID 86667491, compound

https://huagongshe.com/reaction/2368045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68759724HCID 68759724—
SolventDichloromethaneHCID 6344—
ProductHCID 86667491HCID 86667491—

Reaction Conditions

Temperature5 °C

Reaction Steps

3-[(4-Bromo-phenyl)-cyclopropyl-methyl]-6-(2-methyl-allyl)-6-phenyl-[1,3]oxazinan-2-one (diastereomer 2 from Step 3; 1.60 g) dissolved in dichloromethane (15 mL) was added to a solution of 3-chloroperoxybenzoic acid (77%, 0.94 g) in dichloromethane (15 mL) cooled to 5° C. The solution was stirred at room temperature for 3 h, before another portion of 3-chloroperoxybenzoic acid (77%, 0.13 g) was added. After stirring the solution at room temperature for another 1.5 h, aqueous 10% Na2S2O3 solution (10 mL) and aqueous saturated NaHCO3 solution (10 mL) were added and the resulting mixture was stirred for further 30 min. Dichloromethane (20 mL) was added and the organic phase was separated and washed with a 1:1 mixture of aqueous 10% Na2S2O3 solution and aqueous saturated NaHCO3 solution. Then the organic phase was washed with water, dried (MgSO4), and concentrated to furnish the title compound. Yield: 1.86 g (ca. 85-90% pure, quantitative); LC-MS (Method 1): tR=4.00 min; Mass spectrum (ESI+): m/z=456/458 (Br) [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703765B2
Source datasetuspto-grants-2014_04
ORD IDord-6e717cb860a24f818a65e6140c773ea5
Source noteuspto-grants-2014_04