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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1977595Erstellt: 26. Oktober 2026

Acetic Acid → N-Benzylcytisine

https://huagongshe.com/reaction/1977595

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBenzaldehydeHCID 240—
EduktCytisineHCID 10235—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktN-BenzylcytisineHCID 87291258%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06235734B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-38950696e7234e45a9a56d5782406ba5
Quellennotizuspto-grants-2001_05