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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706863Generated: October 30, 2026

Chlorosulfonic acid → HCID 53719869, compound

https://huagongshe.com/reaction/1706863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantBenzene, 1-methyl-2-octylHCID 524675—
SolventDiethyl EtherHCID 3283—
ProductHCID 53719869HCID 53719869—

Reaction Steps

Octyltoluene (50 g.-0.245 mole) as prepared in Table 1 was added slowly at 5°-10° C. with stirring over one half hour (some exotherm) to 81 g. (0.69 mole) chlorosulfonic acid in a 250 ml. round bottom flask fitted with air stirrer, thermometer, addition funnel, reflux condenser, scrubber and ice bath. The reaction mixture was allowed to stir for three hours at 25°-30° C. and then stand overnight. It was poured onto 900 g. ice, 500 ml. diethyl ether was added and the mixture was stirred until the ice melted. The resulting organic phase was washed with water, 30% aqueous Na2CO3, again with water, dried over Na2SO4 and the solvent was evaporated. Thirty nine g. of octylmethylbenzenesulfonyl chloride was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209419
Source datasetuspto-grants-1980_06
ORD IDord-bcef854516ff4245ae00ea39c64d9d61
Source noteuspto-grants-1980_06