반응 #1108078

ord-3b406eda9a7c461eb3620349dc1afc08

반응 방정식

C1=C(c2cc3ccccc3[nH]2)CCC1
2-(Cyclopenten-1-yl)indole
CCOC(=O)/C=C\C#N
ethyl cis-3-cyanoacrylate
CCOC(=O)C1c2c([nH]c3ccccc23)C2=C(CCC2)C1C#N
ethyl 4-cyano-1,2,3,4,5,10-hexahydrocyclopenta[a]carbazole-5-carboxylate
수율 8.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The volatiles were removed by kugelrohr distillation at 110° C.
  2. 2
    기타0.8 mm to afford 19.7 g of an amber-brown tar

실험 절차

2-(Cyclopenten-1-yl)indole (13.6 g, 74 mmol), ethyl cis-3-cyanoacrylate (17.8 g, 142 mmol) and BHT (70 mg) were heated to 180° C. under nitrogen for 30 min. The volatiles were removed by kugelrohr distillation at 110° C. and 0.8 mm to afford 19.7 g of an amber-brown tar. Addition of ether (50 mL) afforded a precipitate of a single isomer of white crystalline ethyl 4-cyano-1,2,3,4,5,10-hexahydrocyclopenta[a]carbazole-5-carboxylate (1.89 g, 8.2% yield); mp 192-195° C. NMR (CDCl3) δ 7.91 (s, 1H), 7.46 (d, 1H), 7.34 (d, 1H), 7.12 (m, 2H), 4.31 (d, 1H0, 4.32 (m, 2H), 4.20 (d, 1H), 3.46 (t, 1H), 3.30 (q, 1H), 2.80 (m, 1H), 2.3-1.4 (m, 6H), 1.34 (t, 3H). Anal. Calcd for C19H20N2O2: C, 74.00; H, 6.54; N, 9.08. Found: C, 73.84; H, 6.53; N, 9.03.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08716493B2uspto-grants-2014_05