反応 #79624

ord-2becbd89d9534f82b8abae6f29b19d24

反応方程式

COC(=O)c1cccc(N)c1Cl
methyl 2-chloro-3-aminobenzoate
O=C1CCCC(=O)C1
1,3-cyclohexanedione
COC(=O)c1cccc(NC2=CC(=O)CCC2)c1Cl
3-(3-carbomethoxy-2-chloroanilino)cyclohex-2-en-1-one
収率 84.0%

反応条件

温度
120°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The resultant solid was triturated with hot ethyl acetate
  2. 2
    その他dried in vacuo

実験手順

A mixture of methyl 2-chloro-3-aminobenzoate (11.11 g, 59.86 mM) and 1,3-cyclohexanedione (9.05 g, 80.8 mM) was heated at 120° C. under a stream of nitrogen for 4 hours. The resultant solid was triturated with hot ethyl acetate, then dried in vacuo to afford 14.05 g (84%) of 3-(3-carbomethoxy-2-chloroanilino)cyclohex-2-en-1-one as a yellow orange solid. 1H NMR (CDCl3) δ7.6 (dt, 1H, J=1 and 8 Hz), 7.3 (t, 1H, J=8 Hz), 6.6 (br s, 1H), 5.62 (s, 1H), 3.95 (s, 3H), 2.6 (t, 2H, J=6 Hz), 2.4 (t, 2H, J=6 Hz), and 2.1 (m, 2H). IR (CHCl3, cm−1) 3050, 2950, 1729, 1536, 1351, 1299, 1290, 1267, and 1135. MS (ES) m/e 278, 280, 282.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06713645B1uspto-grants-2004_03