돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349216생성일: 2026년 10월 26일

Triethylamine → N-[(3-chlorophenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amine

https://huagongshe.com/reaction/349216

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-ChlorobenzaldehydeHCID 11477—
반응물Quinuclidine, 3-amino-, dihydrochlorideHCID 197853—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물N-[(3-chlorophenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amineHCID 1715896430%

반응 단계

A mixture of of 3-aminoquinuclidine dihydrochloride (2.0 g, 10.0 mmol), NEt3 (1.3 mL) and 3-chlorobenzaldehyde (1.5 g, 11.0 mmol) in THF (50 mL) was stirred at room temperature. To this was added Na(OAc)3BH 13.2 g, 15 mmol) and the reaction was stirred overnight. The reaction mixture was diluted with 3N NaOH and water and extracted with EtOAc. The organic extracts were combined, washed with water and then brine and dried over K2CO3. The solution was filtered and the solvent was evaporated in vacuo to give an oil which was chromatographed on silica (94/6 CHCl3/0.5 M NH3 in MeOH). The appropriate fractions were combined and the solvent was evaporated in vacuo to give N-[(3-chlorophenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amine (0.75 g, 30%) as an intermediate, a light yellow semi-solid. MH+=251,253. The 1H NMR was consistent with the assigned structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179818B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-91f1822674c442d28b532453a12610e5
출처 메모uspto-grants-2007_02