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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350021Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 21936588, compound

https://huagongshe.com/reaction/1350021

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 21936603HCID 21936603—
SolventChloroformHCID 6212—
ProductHCID 21936588HCID 21936588100%

Reaction Steps

A solution of tert-butyl 2-[2-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (10.75 g, 29.0 mmol) in 150 mL of CHCl3 was chilled in an ice water bath. The solution was treated with 3-chloroperoxybenzoic acid (MCPBA, 70%, 10.73 g, 43.5 mmol). After stirring for 1.5 h, the reaction mixture was washed with 1% Na2CO3 (3×) solution and the layers were separated. The organic portion was washed with H2O and brine then dried over Na2SO4 and concentrated to give a sticky brown solid. The solid was triturated with ether to yield 11.21 g of tert-butyl 2-[2-(2-methyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate as a light tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214675B2
Source datasetuspto-grants-2007_05
ORD IDord-83d3c145b37547769f53627bd54a2b4c
Source noteuspto-grants-2007_05