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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426004Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 86696139, compound

https://huagongshe.com/reaction/1426004

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 66735700HCID 66735700—
SolventDichloromethaneHCID 6344—
ProductHCID 86696139HCID 86696139—

Reaction Steps

m-Chloroperbenzoic acid (455 mg) was added to a solution of 3-[(S)-1-(4-bromophenyl)-ethyl]-6-(cyclopropylmethyl)-6-(2-methylallyl)-1,3-oxazinan-2-one (516 mg) in CH2Cl2 (15 mL) at 0° C. The mixture was stirred at room temperature overnight. The mixture was then washed with 3% aqueous Na2S2O3 solution and saturated aqueous NaHCO3 solution. The aqueous washing phase was extracted with ethyl acetate (3×30 mL) and the combined organic layer was washed with brine, dried (Na2SO4), and concentrated to afford the crude title compound which was used without further purification. Yield: 490 mg (91% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933072B2
Source datasetuspto-grants-2015_01
ORD IDord-368f1675a7e1459ab3e5b13c78223d12
Source noteuspto-grants-2015_01