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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728529Generated: October 30, 2026

Benzenesulfonyl chloride, 4-chloro-3-nitro- → 4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamide

https://huagongshe.com/reaction/728529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
ReactantTriethylamineHCID 8471—
ReactantN-MethyloctadecylamineHCID 75539—
SolventChloroformHCID 6212—
Product4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamideHCID 1975371171.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In 300 ml of chloroform, 100 g of 4-chloro-3-nitrobenzenesulfonyl chloride was dissolved, and cooled to 0° C. Thereto, a solution of 84.3 g of methyloctadecylamine in chloroform was added dropwise. Then, 39.5 g of triethylamine was added dropwise as the reaction system was kept at a temperature from 0° C. to 10° C. After the conclusion of the addition, the reaction was run for 1 hour. Then, the solvent was distilled away, and the residue was dissolved in 500 ml of methanol under heating. The solution was allowed to stand for a while in order to cool. Thereupon, crystals separated out, and they were filtered off. Yield: 109 g, Percent yield: 71.2%, Melting point: 86°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049477
Source datasetuspto-grants-1991_09
ORD IDord-92043e01933842cba172fbe0064fe547
Source noteuspto-grants-1991_09