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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1365124Erstellt: 23. Oktober 2026

tert-Butanol → tert-butyl N-(furan-3-yl)carbamate

https://huagongshe.com/de/reaction/1365124

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
Edukt3-Furoic acidHCID 10268—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Produkttert-butyl N-(furan-3-yl)carbamateHCID 1220718676%

Reaktionsschritte

3-Furoic acid (5.60 g, 1.0 eq) was dissolved in tert-butanol (200 ml) and treated with triethylamine (10 ml, 1.4 eq) and diphenyl phosphoryl azide (12 ml, 1.1 eq). Mixture was heated at reflux for 18 h. Reaction mixture was cooled to room temperature, then concentrated to 50 ml and poured into saturated aq. NaHCO3. Mixture was stirred at 0° C. for 2 h. Solid was collected by filtration and dried under high vacuum. The crude reaction mixture was purified by flash chromatography to yield tert-butyl furan-3-ylcarbamate 32 (6.95 g, 76%): 1H NMR (CDCl3, 400 MHz) δ 7.71 (bs, 1H), 7.27 (m, 1H), 6.27 (bs, 1H), 6.20 (bs, 1H), 1.50 (s, 9H); MS (Q1) 184 (M)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07888352B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-0c15e11db48b49feb4d31a6aa48d9716
Quellennotizuspto-grants-2011_02