反応 #2146725

ord-f19f1971db63476a9a8a5c58624856a3

反応方程式

COC(=O)c1cc(N)cc(C(=O)OC)c1
dimethyl 5-aminoisophthalate
CC(=O)CCC(C)=O
acetonylacetone
COC(=O)c1cc(C(=O)OC)cc(-n2c(C)ccc2C)c1
9
収率 92.0%
COC(=O)c1cc(C(=O)OC)cc(-n2c(C)ccc2C)c1
Dimethyl 5-(2,5-dimethyl-1H-pyrrol-1-yl)isophthalate
収率 92.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was heated in a Dean-Stark apparatus
  2. 2
    温度under reflux for 12 h
  3. 3
    濃縮the mixture was concentrated with a rotary evaporator
  4. 4
    その他the resulting brown oil was purified by flash column chromatography (EtOAc/hexanes, 1:19-1:9)

実験手順

To a solution of dimethyl 5-aminoisophthalate (8, 10.5 g, 50 mmol) in toluene (50 mL) was added acetonylacetone (6.18 mL, 52.5 mmol) and p-TsOH (95 mg, 0.5 mmol). The reaction mixture was heated in a Dean-Stark apparatus under reflux for 12 h. After cooling to room temperature, the mixture was concentrated with a rotary evaporator, and the resulting brown oil was purified by flash column chromatography (EtOAc/hexanes, 1:19-1:9) to give 9 (13.2 g, 46 mmol, 92%) as a white solid: 1H NMR (500 MHz, CDCl3) δ 2.05 (s, 6H), 3.99 (s, 6H), 5.95 (s, 2H), 8.11 (s, 2H), 8.74 (s, 1H); 13C NMR (125 MHz, CDCl3) δ 13.3, 52.9, 106.8, 128.9, 130.0, 132.0, 133.6, 139.9, 165.7; LC-MS (M +H+) calcd for C16H18NO4 288, found 288.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08278084B2uspto-grants-2012_10