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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1919723생성일: 2026년 10월 25일

Dimethyl Sulfate → N-Boc-2-Ethyl-6-methylPiperidine

https://huagongshe.com/reaction/1919723

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참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물tert-Butyl 2-Ethylpiperidine-1-carboxylateHCID 12170201—
반응물CID 53628100HCID 178418400—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물N-Boc-2-Ethyl-6-methylPiperidineHCID 2262014859%

반응 조건

온도-20 °C

반응 단계

A solution of N-Boc-2-ethylpiperidine (1.5 g, 7.0 mmol) in 28 mL of ether was cooled to −60° C. and treated with TMEDA (1.6 mL, 10.85 mmol), followed by sec-BuLi (8.5 mL, 10.85 mmol) dropwise. The mixture was slowly warmed to −20° C., stirred for 30 min, and then cooled to −78° C. The mixture was treated with a solution of dimethyl sulfate (1.6 mL, 16.69 mmol) in ether and slowly warmed to room temperature. The mixture was diluted with water and then extracted with ether. The combined extracts were dried over K2CO3 and concentrated to give a crude product as an oil which was chromatographed on silica with 5% EtOAc/hexane to give 0.88 g (59%) of the product which was homogeneous by TLC analysis. 1H NMR (250 MHz) δ 3.91-3.87 (m, 1H), 3.69-3.65 (m, 1H), 1.83-1.41 (m, 17H), 1.21-1.19 (d, 3H), 0.85-0.82 (t, 3H); 13C NMR (62.7 MHz) 155.2 (s), 78.6 (s), 53.0 (s), 46.8 (s), 28.5 (s), 27.2 (s), 26.7 (s), 22.4 (s), 20.7 (s), 13.4 (s), 11.4 (s) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08168657B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-a2c66eea1a8b437ea6a106e794bad348
출처 메모uspto-grants-2012_05