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

HRID 400401
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HRID 400401 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
85 °C

실험 절차

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)+.

후처리

  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)

출처 및 근거

ORD 기록
ord-45a4b15e192f4df8b23ceb5b9c53d85d
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08741898B2

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