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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368866Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 18722386, compound

https://huagongshe.com/reaction/1368866

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 9818617HCID 9818617—
SolventDichloromethaneHCID 6344—
ProductHCID 18722386HCID 1872238666%

Reaction Steps

To a solution of 3-bromo-8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one (2 g) (6.2 mmoles) in anhydrous dichloromethane (14 ml) at 0° C. and under an argon atmosphere, was added a solution of 3-chloroperbenzoic acid (1.76 g) (10.4 mmoles) in anhydrous dichloromethane (35 ml) dropwise over a period of 30 minutes. The mixture was allowed to warm to room temperature and after 18 h additional 3-chloroperbenzoic acid (0.88 g) (5.2 mmoles) in anhydrous dichloromethane (25 ml) was added and the mixture was stirred for a total of 42 h. The mixture was diluted with dichloromethane and washed with 1N NaOH (200 ml). The aqueous layer was extracted with additional dichloromethane (2X200 ml) and the combined organic layers were dried over magnesium sulfate, filtered and evaporated to dryness. The product was chromatographed on silica gel using 0.25%-0.5%-1% (10% conc. NH4OH in methanol)dichloromethane as the eluant to give the title compound (Yield:1.386 g, 66%): ESIMS; m/z 338.1 (MH+); δc (CDCl3) CH2: 30.5, 34.0; CH: 126.9, 127.6, 130.3, 132.5, 140.4; C: 121.0, 135.1, 138.3, 139.7, 141.6, 145.3, 188.0 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576639B1
Source datasetuspto-grants-2003_06
ORD IDord-13ae8314fbbb466fa79a7b511d1cdc9b
Source noteuspto-grants-2003_06