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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165037Generated: October 31, 2026

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

https://huagongshe.com/reaction/2165037

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 m(of chloroform was added to 100 g of 4-chloro-3-nitrobenzenesulfonyl chloride and the mixture was cooled to 0° C. Then, a chloroform solution containing 84.3 g of methyloctadecylamine was added dropwise to the mixture. After 39.5 g of triethylamine was added dropwise thereto while the temperature was kept at 0° to 10° C.., the mixture was stirred for 1 hour at room temperature. The chloroform was distilled off under reduced pressure, then 500 ml of methanol was added to the residue, and it was heated to dissolve the residue. The mixture was cooled to precipitate crystals and the crystals were filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939066
Source datasetuspto-grants-1990_07
ORD IDord-464be7488b754ddda807d8eaf0ed5941
Source noteuspto-grants-1990_07