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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 840680생성일: 2026년 10월 26일

Dimethyl Sulfate → N-Boc-2-Methyl-Piperidine

https://huagongshe.com/reaction/840680

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물N-(tert-butoxycarbonyl)piperidineHCID 7010304—
반응물CID 53628100HCID 178418400—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물N-Boc-2-Methyl-PiperidineHCID 457807799.2%

반응 조건

온도-78 °C

반응 단계

A solution of N-Boc-Piperidine (15.0 g, 80.95 mmol) in ether (160 mL) was cooled to −78° C. and treated with TMEDA (15.9 mL, 105.2 mmol) followed by sec-BuLi (85 mL, 105.2 mmol) dropwise. The mixture was stirred for 3 h at −78° C. and then treated with a solution of dimethyl sulfate (15.3 mL, 161.9 mmol) in 65 mL of ether. The mixture was warmed to room temperature and then was diluted with water and extracted with ether. The combined extracts were dried over K2CO3 and then concentrated to give a crude product as a colorless oil. The product was purified by column chromatography on silca gel with 5% EtOAc/hexane to afford 16.0 g (81%) of product as a clear oil which was homogeneous by TLC analysis. 1H NMR (300 MHz) 67 4.33 (m, 1 H), 3.92-3.81 (pair of br. d, 1 H), 2.81-2.72 (dt, 1H), 1.60-1.36 (m, 15 H), 1.09-1.07 (d, 3 H); 13C NMR (75 MHz) 154.9 (s), 78.6 (s), 45.9 (s), 38.6 (s), 29.9 (s), 28.4 (s), 25.6 (s), 18.6 (s), 15.6 (s), ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06369078B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-04bcec3d8e0849d38352a346ae5610cd
출처 메모uspto-grants-2002_04