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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 881233Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/881233

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
PatentnummerUS08993563B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-9a2169d12f524c01afbeca9f6dd47afb
Quellennotizuspto-grants-2015_03