反応 #487583

ord-45a4b15e192f4df8b23ceb5b9c53d85d

反応方程式

COC(=O)C1Cc2ccccc2CC(C(=O)OC)C1=O
dimethyl 7-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-6,8-dicarboxylate
[K+].[OH-]
KOH
O=C1CCc2ccccc2CC1
8,9-dihydro-5H-benzo[7]annulen-7(6H)-one
収率 57.0%

溶媒

反応条件

温度
85°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After cooling to ambient temperature
  2. 2
    その他the volatiles were evaporated
  3. 3
    workup.ADDITIONTo the residue was added 120 mL of 2N HCl at 0° C.
  4. 4
    抽出the crude product was extracted by EtOAc (200 mL×2)
  5. 5
    洗浄The combined extracts were washed with brine
  6. 6
    乾燥After being dried (MgSO4)
  7. 7
    ろ過filtered
  8. 8
    濃縮concentrated
  9. 9
    その他the residue was purified by flash column chromatography on silica gel (hexanes/EtOAc 8:1)

実験手順

The crude dimethyl 7-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-6,8-dicarboxylate was dissolved in 200 mL of ethanol (EtOH) and then 100 mL of 2 N KOH. The resulting mixture was refluxed at 85° C. for 17 h. After cooling to ambient temperature, the volatiles were evaporated. To the residue was added 120 mL of 2N HCl at 0° C., the crude product was extracted by EtOAc (200 mL×2). The combined extracts were washed with brine. After being dried (MgSO4), filtered, and concentrated, the residue was purified by flash column chromatography on silica gel (hexanes/EtOAc 8:1) to afford 6.6 g (57%) of 8,9-dihydro-5H-benzo[7]annulen-7(6H)-one as a white solid: mp 40-41° C.; 1H NMR (300 MHz, CDCl3) δ: 7.21 (m, 4H), 2.94-2.90 (m, 4H), 2.63-2.60 (m, 4H); LC-MS: 161 (M+H)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08741898B2uspto-grants-2014_06