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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1977595생성일: 2026년 10월 26일

Acetic Acid → N-Benzylcytisine

https://huagongshe.com/reaction/1977595

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물BenzaldehydeHCID 240—
반응물CytisineHCID 10235—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
생성물N-BenzylcytisineHCID 87291258%

반응 단계

To a 25 ml round bottom flask was added 0.510 gm (2.68 mmol) cytisine in 10 ml of 1,2-dichloroethane. The above solution was treated with 0.272 ml (2.68 mmol) benzaldehyde, 153 μl acetic acid and 0.852 gm (4.02 mmol) sodium triacetoxyborohydride. The reaction mixture was stirred at room temperature for 2 hours and was then partitioned between methylene chloride and 1 N HCl (aq). The organic phase was washed with brine, dried and the solvent evaporated in vacuo to a solid. Chromatography on silica gel eluting with 1% methanol in methylene chloride afforded 434 mg (58%) of the title product which was used in the next step. 1H NMR (CDCl3, 250 MHz) δ 7.28 (dd, 1H), 7.15 (m, 3H), 6.98 (m, 2H), 6.98 (m, 2H), 6.52 (d, 1H), 5.92 (d, 1H), 4.10 (d, 1H), 3.88 (dd, 1H), 3.40 (dd, 2H), 2.88 (m, 3H), 2.39 (br.s, 1H), 2.3 (dd, 2H), 1.82 (dd, 2H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06235734B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-38950696e7234e45a9a56d5782406ba5
출처 메모uspto-grants-2001_05