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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5126Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/5126

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktEthyl AcetateHCID 8857—
EduktSodium AzideHCID 33557—
Edukt1,8-OctanediolHCID 69420—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt8-Azido-1-octanolHCID 11789665—

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05243035
Quelldatensatzuspto-grants-1993_09
ORD IDord-86a11031d1d743c286db830c75a75df3
Quellennotizuspto-grants-1993_09