Formaldehyde → 3,4-Dihydro-6-methoxy-2-methylene-1(2h)-naphthalenone

HRID 1384963ノート

反応式

HRID 1384963 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[CH2:8][CH2:7][CH2:6]2.C=O.F[C:17](F)(F)C([O-])=O.C[NH2+]C1C=CC=CC=1.CCOCC>C1COCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[C:8](=[CH2:17])[CH2:7][CH2:6]2

参加物

6

反応物 4

HCID 712FormaldehydeHCID 3283Diethyl EtherHCID 141126-Methoxy-alpha-tetraloneHCID 2724109N-Methylanilinium trifluoroacetate

生成物 1

HCID 113444693,4-Dihydro-6-methoxy-2-methylene-1(2h)-naphthalenone

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of 6-methoxytetralone (29.24 g, 165.9 mmol), paraformaldehyde (22.4 g, 746.6 mmol) and N-methylanilinium trifluoroactate (55 g, 248.9 mmol) in 250 mL THF was refluxed for 4 hours and allowed to come to room temperature. To this was added ether (250 mL) with stirring and the mixture was decanted to remove the gummy precipitate. The supernatant was washed with sat. NaHCO3, the oganic layer was dried (MgSO4) and concentrated. The residue was redissolved in ether, filtered through celite and concentrated to afford the title compound as a thick yellow oil.

後処理

  1. temperaturewas refluxed for 4 hours
  2. customto come to room temperature
  3. customthe mixture was decanted
  4. customto remove the gummy precipitate
  5. washThe supernatant was washed with sat. NaHCO3
  6. dry with materialthe oganic layer was dried (MgSO4)
  7. concentrationconcentrated
  8. dissolutionThe residue was redissolved in ether
  9. filtrationfiltered through celite
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-a23a45718bec4f72846622544d638c92
出典データセット
uspto-grants-2001_07
特許番号
US06262068B1

反応ノート

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