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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8639Erstellt: 23. Oktober 2026

4-Toluenesulfonyl chloride → Toluene-4-sulfonic acid 2-[tert-butoxycarbonyl-(3-fluoro-benzyl)-amino]-ethyl ester

https://huagongshe.com/de/reaction/8639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktTriethylamineHCID 8471—
Edukt2-(3-Fluoro-benzylamino)-ethanolHCID 10866749—
Edukttert-butyl N-[(3-fluorophenyl)methyl]-N-(2-hydroxyethyl)carbamateHCID 69653122—
LösungsmittelDichloromethaneHCID 6344—
ProduktToluene-4-sulfonic acid 2-[tert-butoxycarbonyl-(3-fluoro-benzyl)-amino]-ethyl esterHCID 23548235—

Reaktionsschritte

Add p-toluenesulfonyl-chloride (0.71 g, 3.71 mmol), portionwise, to a mixture of (3-fluoro-benzyl)-(2-hydroxy-ethyl)-carbamic acid dimethyl-ethyl ester (1 g, 3.71 mmol, prepared from 2-(3-fluoro-benzylamino)-ethanol by methods as are known in the art), triethylamine (0.751 g, 7.4 mmol) and dichloromethane (6 mL). Stir the resulting suspension vigorously overnight at room temperature. Add water (10 mL), separate the organic layer, and extract the aqueous layer with dichloromethane (5 mL), twice. Combine the organic layers and wash with citric acid (5 mL, 20% in water), dry with sodium sulfate and evaporate the solvent to give the final, desired compound. The final compound may be purified by chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091199B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-3bfb9478b47f4e919a8a0e2f00a8190d
Quellennotizuspto-grants-2006_08