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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115769Generated: November 1, 2026

m-Chloroperbenzoic acid → 4-Benzenesulfinyl-6,7-dimethoxy-quinoline

https://huagongshe.com/reaction/2115769

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67520293HCID 67520293—
SolventDichloromethaneHCID 6344—
Product4-Benzenesulfinyl-6,7-dimethoxy-quinolineHCID 67520538—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 6,7-dimethoxy-4-phenylsulfanyl-quinoline (Step a, 1.0 g, 3.4 mmol) in CH2Cl2 (30 mL) at −78° C., 3-chloroperoxybenzoic acid (0.64 g, 3.7 mmol) was added in CH2Cl2 dropwise slowly. The reaction was stirred at −78° C. for 2 h. The solution was poured into saturated NaHCO3 and extracted with CH2Cl2 3×. The combined organic layer was washed with saturated NaHCO3, water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by silica gel column chromatography with (70-100% EtOAc/Hexane) to give the titled compound as a white solid. MS (ESI, pos. ion) m/z: 314.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-e42c2274ad05476885ea43dcdd94a3f9
Source noteuspto-grants-2008_10