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HRID 535861作成日:2026年10月27日

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

https://huagongshe.com/reaction/535861

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Dimethyl (diazomethyl)phosphonateHCID 5115033—
反応物1-Boc-piperidine-3-carboxaldehydeHCID 9964448—
溶媒MethanolHCID 887—
生成物tert-Butyl 3-ethynylpiperidine-1-carboxylateHCID 21963855100.4%

反応手順

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 (1H, brs), 3.70-3.75 (1H, m), 2.95-3.02 (2H, m), 2.40-2.47 (1H, m), 2.05 (1H, d, J=2.1 Hz), 1.94-1.99 (1H, m), 1.69-1.73 (1H, m), 1.50-1.63 (2H, m), 1.46 (9H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859553B2
出典データセットuspto-grants-2014_10
ORD IDord-fee5f01557c74cd9a77029b6804140ff
出典メモuspto-grants-2014_10