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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874574Generated: October 29, 2026

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

https://huagongshe.com/reaction/874574

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 1 l 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 numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-d6f8cb0e19f6467ea0384c06c4929207
Source noteuspto-grants-2015_03