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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377383Generated: November 3, 2026

4-Chlorobenzenesulfonyl chloride → HCID 54417527, compound

https://huagongshe.com/reaction/1377383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
Reactant1-HexacosanolHCID 68171—
SolventDichloromethaneHCID 6344—
ProductHCID 54417527HCID 5441752722%

Reaction Steps

A solution of hexacosanol (250 mgs, 0.654 mmol), triethylamine (125 1, 0.900 mmol) and 4-chlorobenzenesulphonyl chloride (150 mgs, 0.711 mmol) in methylene chloride (30 ml) is stirred at room temperature for 120 h. The reaction mixture is then diluted with methylene chloride (20 ml) and washed with water (2×50 ml). The organic phase is dried over magnesium sulphate, filtered and concentrated to give a crude product. Flash column chromatography on silica gel (10:1 hexane:ethyl acetate) followed by recrystallization from methanol gives n-hexacosanyl-4-chlorobenzenesulphonate (80 mgs, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665328
Source datasetuspto-grants-1997_09
ORD IDord-11081f1085fe46a4b1a54faa635e9b6f
Source noteuspto-grants-1997_09