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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970006생성일: 2026년 10월 25일

Benzidine → N-1-azabicyclo[2.2.2]oct-3-yl-1,1'-biphenyl-4,4'-diamine

https://huagongshe.com/reaction/970006

반응식

참여 물질

역할이름HCID투입량
반응물BenzidineHCID 7111—
반응물Sodium SulfateHCID 24436—
반응물1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Acetic AcidHCID 176—
생성물N-1-azabicyclo[2.2.2]oct-3-yl-1,1'-biphenyl-4,4'-diamineHCID 11380826—

반응 단계

3-Quinuclidinone hydrochloride (Aldrich, 1.61 g, 10 mmol) in acetic acid (25 mL) was treated with biphenyl-4,4′-diamine (Aldrich, 0.92 g, 5.0 mmol), Na2SO4 (anhydrous, Aldrich, 7.40 g, 50 mmol) and NaBH(OAc)3 (Aldrich, 3.16 g, 15 mmol) at ambient temperature for 15 hours. The reaction mixture was slowly poured into a flask containing 75 mL of saturated NaHCO3, stirred for 20 minutes, and extracted with ethyl acetate (3×100 mL). The extracts were combined and washed with brine (2×20 mL). The organic phase was concentrated under reduced pressure and the title compound was purified by chromatography (SiO2, CH2Cl2:MeOH:NH3.H2O, 80:20:4, Rf. 0.10) as a solid (0.98 g, yield, 67%). 1H NMR (MeOH-d4, 300 MHz) δ 1.40-1.52 (m, 1H), 1.64-1.84 (m, 2H), 1.89-2.04 (m, 2H), 2.57 (ddd, J=13.9, 5.2, 2.1 Hz, 1H) 2.75-3.00 (m, 4H), 3.27-3.35 (m, 1H), 3.50-3.60 (m, 1H), 6.61-6.69 (m, 2H), 6.80-6.86 (m, 2H), 6.92-6.97 (m, 2H), 7.06-7.13 (m, 2H) ppm. MS (DCl/NH3) m/z 294 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07309699B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-3035ec7bf2c24e5a8b6dcecf6da847f0
출처 메모uspto-grants-2007_12