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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 659131Erstellt: 23. Oktober 2026

Potassium Carbonate → Tert-butyl (1-phenylbut-3-yn-1-yl)carbamate

https://huagongshe.com/de/reaction/659131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktTert-butyl N-(3-oxo-1-phenylpropyl)carbamateHCID 15087934—
Edukt(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
LösungsmittelMethanolHCID 887—
ProduktTert-butyl (1-phenylbut-3-yn-1-yl)carbamateHCID 5742981387,2%

Reaktionsschritte

To the solution of 1.2 g of tert-butyl 3-oxo-1-phenylpropylcarbamate (Formula 12) and 1.38 g of dimethyl 1-diazo-2-oxopropylphosphonate (Formula 15) in 60 mL of methanol at 0° C. was added 1.32 g of potassium carbonate. The mixture was stirred at room temperature for 16 hours then quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. Column chromatography (5% ethyl acetate/hexane) gave 1.03 g (87%) of tert-butyl 1-phenylbut-3-ynylcarbamate (Formula 16) as a white solid. 1H NMR (300 MHz, CDCl3) δ 1.43 (s, 9H), 1.98-2.00 (m, 1H), 2.6-2.8 (m, 2H), 4.88 (br, 1H), 5.16 (br, 1H), 7.23-7.37 (m, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08080570B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-6e95369fee4741a88a46b9b467e411f2
Quellennotizuspto-grants-2011_12