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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636057Generated: October 31, 2026

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

https://huagongshe.com/reaction/1636057

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-Butoxycarbonylamino)propanol (10.0 g) is dissolved in methylene chloride (100 ml), and thereto are added with stirring triethylamine (8.66 g) and tosyl chloride (16.3 g) under ice-cooling, and the reaction mixture is stirred at room temperature overnight. The reaction mixture is concentrated, and the residue is dissolved in a mixture of water and ethyl acetate. The organic layer is separated, washed with a saturated sodium chloride solution, dried over sodium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography to give the title compound (15.37 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06512118B1
Source datasetuspto-grants-2003_01
ORD IDord-296584cdd8e644a9b0ff397c306c5a29
Source noteuspto-grants-2003_01