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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084595Generated: October 30, 2026

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

https://huagongshe.com/reaction/2084595

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 numberUS06716983B2
Source datasetuspto-grants-2004_04
ORD IDord-d2538baefe51434e82388829d1d4ed7a
Source noteuspto-grants-2004_04