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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472133Generated: October 29, 2026

Oxalyl chloride → 4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride

https://huagongshe.com/reaction/472133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantSodiumHCID 5360545—
Reactant4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonic acidHCID 21963051—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochlorideHCID 8660786592%

Reaction Conditions

Temperature-10 °C

Reaction Steps

76 g (216 mmol) of the sodium salt of 4-(2-methylquinolin-4-ylmethoxy)benzenesulfonic acid in 500 ml of dimethylformamide are added dropwise to a solution of 55 ml (649 mmol) of oxalyl chloride in 100 ml of dichloromethane, cooled beforehand to −10° C. After the addition, the reaction medium is stirred at ambient temperature for 18 h. The reaction medium is then poured into 11 of ice and then extracted with ethyl acetate. The organic phases are combined, washed with water and then with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated under vacuum. 77 g (92%) of 4-(2-methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride are obtained in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633196B2
Source datasetuspto-grants-2014_01
ORD IDord-3d6d395d09a94c4fb946ac3ffac1571b
Source noteuspto-grants-2014_01