Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500896Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 85405172, compound

https://huagongshe.com/reaction/1500896

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBenzyl cyclopent-3-en-1-ylcarbamateHCID 10751243—
SolventDichloromethaneHCID 6344—
ProductHCID 85405172HCID 85405172152%

Reaction Steps

To a solution of benzyl cyclopent-3-en-1-ylcarbamate (920 mg, 4.23 mmol) in DCM (20 mL), was added m-CPBA (2.0 g, 7.6 mmol) in portions at 0° C. The mixture was warmed up to RT and stirred at RT for 2 hours. The reaction was quenched by addition of sat. aqueous solution of K2CO3, and the resulting mixture was extracted with DCM (20 mL×3). The combined organic layers were dried over Na2SO4, and then concentrated in vacuo to afford the crude benzyl 6-oxabicyclo[3.1.0]hex-3-ylcarbamate (1.5 g), which was used in the next step directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206191B2
Source datasetuspto-grants-2015_12
ORD IDord-6e47dd6540cc4e14b501fa87b92f79ec
Source noteuspto-grants-2015_12