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Potassium Hydroxide → 5,6,8,9-Tetrahydro-7H-benzo(7)annulen-7-one

HRID 400401
ノート
印刷プレビュー

反応式

HRID 400401 の反応式
[O:1]=[C:2]1[CH:8](C(OC)=O)[CH2:7][C:6]2[CH:13]=[CH:14][CH:15]=[CH:16][C:5]=2[CH2:4][CH:3]1C(OC)=O.[OH-].[K+]>C(O)C>[CH:13]1[C:6]2[CH2:7][CH2:8][C:2](=[O:1])[CH2:3][CH2:4][C:5]=2[CH:16]=[CH:15][CH:14]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 11832654Dimethyl 7-oxo-6,7,8,9-tetrahydro-5h-benzo[7]annulene-6,8-dicarboxylate

生成物 1

HCID 122344855,6,8,9-Tetrahydro-7H-benzo(7)annulen-7-one収率 57%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
85 °C

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)+.

後処理

  1. temperatureAfter cooling to ambient temperature
  2. customthe volatiles were evaporated
  3. additionTo the residue was added 120 mL of 2N HCl at 0° C.
  4. extractionthe crude product was extracted by EtOAc (200 mL×2)
  5. washThe combined extracts were washed with brine
  6. dry with materialAfter being dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customthe residue was purified by flash column chromatography on silica gel (hexanes/EtOAc 8:1)

出典と根拠

ORDレコード
ord-45a4b15e192f4df8b23ceb5b9c53d85d
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08741898B2

反応ノート

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