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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 706846Erstellt: 24. Oktober 2026

Potassium Carbonate → tert-Butyl 3-ethynylpiperidine-1-carboxylate

https://huagongshe.com/de/reaction/706846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktDimethyl (diazomethyl)phosphonateHCID 5115033—
Edukt1-Boc-piperidine-3-carboxaldehydeHCID 9964448—
LösungsmittelMethanolHCID 887—
Produkttert-Butyl 3-ethynylpiperidine-1-carboxylateHCID 21963855100,4%

Reaktionsschritte

A solution of 1-BOC-3-formylpiperidine (1.46 g, 6.85 mmol) and (diazomethyl) phosphonic acid dimethyl ester (1.79 g, 11.94 mmol) in 50 mL methanol was stirred at ice-bath for 10 min, K2CO3 (1.96 g, 14.2 mmol) was added to the above mixture and stirred at ice-bath for 2 hrs, then stirred at rt overnight. The mixture was evaporated in vacuo, to the residue was added EtOAc and water, the organic layer was separated and water layer was extracted with EtOAc (100 mL×3). The combined organic layers were washed with water and brine successively, dried with Na2SO4, filtered, and the filtrate was evaporated in vacuo to give 1.44 g product as colorless oil (100.0%). 1H NMR (300 MHz, CDCl3) δ: 3.90 (1 H, brs), 3.70-3.75 (1 H, m), 2.95-3.02 (2 H, m), 2.40-2.47 (1 H, m), 2.05 (1 H, d, J=2.1 Hz), 1.94-1.99 (1 H, m), 1.69-1.73 (1 H, m), 1.50-1.63 (2 H, m), 1.46 (9 H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09174996B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-32f7a68dc27044bbbc74af035265a9c7
Quellennotizuspto-grants-2015_11