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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727738Generated: October 31, 2026

Chloroform → 4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamide

https://huagongshe.com/reaction/727738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
ReactantN-MethyloctadecylamineHCID 75539—
SolventTriethylamineHCID 8471—
Product4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamideHCID 19753711—

Reaction Conditions

Temperature0 °C

Reaction Steps

300 ml of chloroform was added to 100 g of 4-chloro-3-nitrobenzenesulfonyl chloride. The solution was then cooled to a temperature of 0° C. A chloroform solution of 84.3 g of methyloctadecylamine was added dropwise to the solution. 39.5 g of triethylamine was then added dropwise to the solution while the temperature thereof was kept at 0° to 10° C. The solution was stirred at room temperature for 1 hour. Chloroform was removed from the solution under reduced pressure. 500 ml of methanol was added to the residue. The reaction mixture was heated to complete dissolution. The solution was cooled., The resulting crystals were filtered off and dried. (Yield: 109 g (71%); m.p.: 86°-87° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0000963
Source datasetuspto-grants-1991_09
ORD IDord-6e993effdf964c4fad692a00f31a6c69
Source noteuspto-grants-1991_09