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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828953Generated: November 2, 2026

4-Toluenesulfonyl chloride → 3-[(tert-Butoxycarbonyl)amino]propyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/1828953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactanttert-butyl N-(3-hydroxypropyl)carbamateHCID 3838134—
SolventDichloromethaneHCID 6344—
Product3-[(tert-Butoxycarbonyl)amino]propyl 4-methylbenzene-1-sulfonateHCID 1312030282%

Reaction Steps

3-t-Butoxycarbonylaminopropanol (10.0 g) is dissolved in methylene chloride (100 ml) and thereto are added triethylamine (8.66 g) and tosyl chloride (16.3 g) with stirring under ice cooling. The mixture is stirred at room temperature overnight. The reaction mixture is concentrated and the residue is dissolved in water-ethyl acetate, and the organic layer is separated, washed with an aqueous saturated saline solution, dried over sodium sulfate, and then distilled off the solvent. The residue is purified with a silica gel column chromatography to give 3-t-butoxycarbonylaminopropyl tosylate (15.37 g) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060832B2
Source datasetuspto-grants-2006_06
ORD IDord-58cae1b53b2f4588b4516f1de3c5e035
Source noteuspto-grants-2006_06