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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660822Erstellt: 25. Oktober 2026

tert-Butanol → 2-benzyloxy-4-chloro-N-tert-butoxycarbonylaniline

https://huagongshe.com/reaction/660822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt2-(Benzyloxy)-4-chlorobenzoic acidHCID 22452154—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-benzyloxy-4-chloro-N-tert-butoxycarbonylanilineHCID 22010963—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a solution of 2-benzyloxy-4-chlorobenzoic acid (12.9 g, 46.6 mmol), t-butanol (17.5 mL, 186 mmol) and triethylamine (7.79 mL, 55.9 mmol) in toluene (250 mL) is added DPPA (11.1 mL, 51.3 mmol) and the mixture is stirred at 85° C. for 3 h then at 65° C. for 48 h. The mixture is diluted with EtOAc (500 mL) and is washed with 1N HCl (3×150 mL), NaHCO3 (3×150 mL) and brine (150 mL). The organic phase is dried over sodium sulfate and the solvent evaporated to give a brown solid which is triturated with hexane to give the title compound: (M−1)−=332.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084448B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-d9458652188140359ec8df881f4c9e69
Quellennotizuspto-grants-2011_12