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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576971Generated: October 30, 2026

Methanesulfonyl chloride → HCID 54542349, compound

https://huagongshe.com/reaction/1576971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 3303868HCID 3303868—
SolventBenzeneHCID 241—
ProductHCID 54542349HCID 5454234962.1%

Reaction Steps

In a second synthesis, 10 g of 4-methylbenzohydroximoyl chloride, 6.7 g of methanesulfonyl chloride, and 160 ml of benzene were mixed in a 250-ml, three-necked, round-bottomed flask equipped with a stirrer, thermometer, and drying tube. Triethylamine (8.8 g) was added dropwise during 6 minutes at 5°-10°, and the mixture was stirred at that temperature for 1 hour. The reaction mixture was filtered, the solid was washed with benzene, the washes and filtrate were combined and concentrated, and the concentrate was recrystallized from ethanol to give 9 g of N-(methanesulfonyloxy)-4-methylbenzimidoyl chloride, m.p. 100°-102°. The ir spectrum was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03983246
Source datasetuspto-grants-1976_09
ORD IDord-44cf84dc2d594cc39b56c1b42bd0fd1e
Source noteuspto-grants-1976_09