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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277473Erstellt: 25. Oktober 2026

tert-Butanol → Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate

https://huagongshe.com/reaction/277473

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt2-(Methoxycarbonyl)-6-nitrobenzoic acidHCID 4399477—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoateHCID 996596870%

Reaktionsschritte

To a solution of methyl 2-carboxy-3-nitrobenzoate (7.23 g) in DMF (50 ml) was added diphenylphosphoryl azide (11.3 g) at room temperature and then triethylamine (6.7 ml) was added dropwise to the stirred reaction mixture. After stirring at room temperature for 3 hours, tert-butanol (54 ml) was added to the stirred reaction mixture. After stirring at room temperature for 30 min., the reaction mixture was gradually warmed, then heated under reflux for 1 hour and evaporated to dryness. The resultant residue was dissolved in ethyl acetate, washed with dilute hydrochloric acid, aqueous sodium bicarbonate, and water, and then dried. After evaporation of the solvent, methanol was added to the resultant residue and the mixture was cooled to give colorless crystals (6.7 g, 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355808B2
Quelldatensatzuspto-grants-2002_03
ORD IDord-4723d4e40abd4626a06a0e8d0ea5ab3b
Quellennotizuspto-grants-2002_03