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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5126Generated: October 25, 2026

4-Toluenesulfonyl chloride → 8-Azido-1-octanol

https://huagongshe.com/reaction/5126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantEthyl AcetateHCID 8857—
ReactantSodium AzideHCID 33557—
Reactant1,8-OctanediolHCID 69420—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product8-Azido-1-octanolHCID 11789665—

Reaction Conditions

Temperature10 °C

Reaction Steps

14.65 g of 1,8-octanediol was dissolved in 80 g of pyridine, and cooled to 10° C. A solution of 19 g p-toluenesulfonyl chloride in 70 ml anhydrous methylene chloride was added dropwise thereto, and the mixture was heated gradually overnight for reaction. After water washing, the solvent was removed by distillation, to produce an oily residue. The residue was dissolved in dimethylformamide to a 200 ml solution, to which was added 20 g of sodium azide, and the resultant mixture was maintained at 80° C. for 2 hours for reaction. The mixture was, after added with ethyl acetate, was washed with water 4 times and the solvent was removed by distillation. The object compound was isolated by silica-gel column-chromatography (CHCl3 -AcOEt 5:1-1:1) The yield was 6.07 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05243035
Source datasetuspto-grants-1993_09
ORD IDord-86a11031d1d743c286db830c75a75df3
Source noteuspto-grants-1993_09