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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419945Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 53948112, compound

https://huagongshe.com/reaction/1419945

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-allyl-2-fluoroanisoleHCID 2759004—
SolventDichloromethaneHCID 6344—
ProductHCID 53948112HCID 5394811237.3%

Reaction Steps

4-Allyl-2-fluoro-1-methoxy benzene (1.2 g, 7.22 mmol) was dissolved in CH2Cl2 (35 ml) and treated successively with buffer pH=7.95 (35 ml, NaH2PO4 --Na2HPO4) and m-chloroperbenzoic acid 70% (2.2 g, 9 mmol). Reaction mixture was stirred at room temperature for 63 hours. The aqueous phase was extracted with CH2Cl2 (4×30 ml), combined organic phases were washed with sat. NaHCO3 (50 ml), dried over Na2SO4 and concentrated. The residue was chromatographed over siliga gel (hexan-ethyl acetate 9:1) to provide (RS)-2-(3-Fluoro-4-methoxy-benzyl)-oxirane (0.49 g, 37%) as a yellow oil MS: m/e=182 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889026
Source datasetuspto-grants-1999_03
ORD IDord-84a62dc20abd4ba69c05f754ecdf3a9c
Source noteuspto-grants-1999_03