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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323135Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/323135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt2-(Benzyloxy)-4-chlorobenzoic acidHCID 22452154—
LösungsmittelBenzeneHCID 241—
Produkt2-benzyloxy-4-chloro-N-tert-butoxycarbonylanilineHCID 22010963—

Reaktionsschritte

2-Benzyloxy-4-chlorobenzoic acid (3.0 g) was heated under reflux in a mixture of benzene and t-butyl alcohol. Diphenylphosphoryl azide (3.14 g) and triethylamine (1.21 g) were added in one batch to the mixture and reflux was continued for a further 8 hours. Benzene was removed under reduced pressure and the residue taken up in ethyl acetate. An insoluble white solid was removed by filtration. The remaining organic filtrate was washed successively with diluted hydrochloric acid, water, saturated aqueous sodium hydrogen carbonate and brine. The organic layer was dried over magnesium sulfate and the solvent was evaporated to give 2-benzyloxy-4-chloro-N-tert-butoxycarbonylaniline (1.6 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211242B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-2e09c12c1f6b4a26b67542010047bcc9
Quellennotizuspto-grants-2001_04