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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 215952생성일: 2026년 10월 25일

Triethylamine → HCID 178525098, 화합물

https://huagongshe.com/reaction/215952

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-Benzyl 4-methyl 4-(2-oxoethyl)piperidine-1,4-dicarboxylateHCID 58893182—
반응물HCID 178479277HCID 178479277—
용매1,2-DichloroethaneHCID 11—
용매DichloromethaneHCID 6344—
생성물HCID 178525098HCID 17852509872.4%

반응 단계

A mixture of 1-benzyl 4-methyl 4-(2-oxoethyl)piperidine-1,4-dicarboxylate (4.80 g, 0.0150 mol), cis-4-aminocyclohexanol hydrochloride (2.5 g, 0.016 mol) and triethylamine (3.3 mL, 0.024 mol) in 1,2-dichloroethane (30.0 mL) was stirred at room temperature for 30 min. To the mixture was added sodium triacetoxyborohydride (7.9 g, 0.038 mol) with stirring. The mixture was stirred at room temperature for 1 h, then was heated at 80° C. for 2 h. After cooling, the mixture was diluted with dichloromethane, and washed with IN HCl solution, NaHCO3 (7.5%), water, and brine successively, dried over Na2SO4, filtered, and concentrated. The residue was purified by flash chromatography to give benzyl 2-(cis-4-hydroxycyclohexyl)-1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate (4.20 g, 72.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193207B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-af0a5c1b5a764d38b93dc828e33884af
출처 메모uspto-grants-2012_06