돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 706846생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/706846

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Dimethyl (diazomethyl)phosphonateHCID 5115033—
반응물1-Boc-piperidine-3-carboxaldehydeHCID 9964448—
용매MethanolHCID 887—
생성물tert-Butyl 3-ethynylpiperidine-1-carboxylateHCID 21963855100.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09174996B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-32f7a68dc27044bbbc74af035265a9c7
출처 메모uspto-grants-2015_11