Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715844Generated: November 2, 2026

6-Methoxy-m-toluenesulfonyl chloride → 1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/1715844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-m-toluenesulfonyl chlorideHCID 145149—
ReactantMethyl 1,2,3,4-tetrahydroquinoline-7-carboxylateHCID 16244389—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carboxylic acid methyl esterHCID 68432605—

Reaction Steps

A solution of 1,2,3,4-tetrahydro-quinoline-7-carboxylic acid methyl ester (23.00 g, 0.12 mol) in dichloromethane (0.70 L) and pyridine (0.10 L) was treated with 2-methoxy-5-methyl-benzenesulfonyl chloride (31.78 g, 0.14 mol) and the mixture stirred at room temperature for 18 hours. The reaction mixture was then washed with 0.5 N HCl (0.40 L), water (2 times 0.40 L) and brine (0.25 L) and the organic phase dried over sodium sulphate and evaporated. The residue was sonicated in ether/dichloromethane 95:5 and the precipitate filtered and dried under vacuum. 1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carboxylic acid methyl ester was obtained as an off-white solid, 42.05 g (93%), MS (ISP): m/e=376.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799933B2
Source datasetuspto-grants-2010_09
ORD IDord-c4a6d435aec04483bb9b8b2d6eda8fb7
Source noteuspto-grants-2010_09