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1,1-Dimethylhydrazine → 4-{[3-Methyl-6-(methyloxy)-2-phenyl-1-naphthalenyl]oxy}benzonitrile

HRID 1992984
ノート
印刷プレビュー

反応式

HRID 1992984 の反応式
[CH3:1][C:2]1[C:3]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:4]([O:14][C:15]2[CH:22]=[CH:21][C:18]([CH:19]=O)=[CH:17][CH:16]=2)[C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([O:12][CH3:13])=[CH:7][CH:6]=2.C[N:30](C)N.COS(OC)(=O)=O.C([O-])([O-])=O.[K+].[K+]>CO.O>[CH3:1][C:2]1[C:3]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:4]([O:14][C:15]2[CH:22]=[CH:21][C:18]([C:19]#[N:30])=[CH:17][CH:16]=2)[C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([O:12][CH3:13])=[CH:7][CH:6]=2
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 59761,1-DimethylhydrazineHCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 860871594-[(6-Methoxy-3-methyl-2-phenyl-1-naphthyl)oxy]benzaldehyde

生成物 1

HCID 685372514-{[3-Methyl-6-(methyloxy)-2-phenyl-1-naphthalenyl]oxy}benzonitrile収率 62%

試薬・触媒・溶媒 2

HCID 887
Methanol
溶媒
HCID 962Water溶媒

実験手順

To a solution of 4-{[3-methyl-6-(methyloxy)-2-phenyl-1-naphthalenyl]oxy}benzaldehyde (8) (0.920 g, 2.5 mmol) in MeOH (25 mL) was added N,N-dimethylhydrazine (0.341 mL, 4.5 mmol). The resultant mixture was stirred at room temperature for 12 h under N2. Reaction mixture was concentrated under reduced pressure and the residue was re-dissolved in CH3CN (25 mL) to which were added dimethylsulfate (0.378 mL, 3 mmol) and K2CO3 (0.415 g, 3 mmol) under N2. The reaction mixture was refluxed for 24 h. Reaction mixture was cooled at room temperature and poured into water (100 mL). Reaction mixture was extracted with EtOAc (3×100 mL). The combined organic layer was washed with brine, dried (Na2SO4) and concentrated under reduced pressure to afford the crude product. The product was purified by column chromatography using hexanes:EtOAc (19:1 to 9:1) as an eluent to afford 0.560 g (62%) of the title compound (237) as an off-white solid. IR (film) 2958, 2225, 1602, 1501, 1235 cm−1. 1H NMR (400 MHz, CDCl3): δ 7.66 (d, J=9.2 Hz, 1H), 7.60 (s, 1H), 7.37 (d, J=6.4 Hz, 2H), 7.29-7.23 (m, 3H), 7.15 (d, J=2.4 Hz, 1H), 7.11 (d, J=1.6 Hz, 1H), 7.09 (d, J=1.6 Hz, 1H), 7.08 and 7.05 (dd, J1=9.2 Hz, J2=2.4 Hz, 1H), 6.64 (d, J=6.8 Hz, 2H), 3.94 (s, 3H), 2.25 (s, 3H). LCMS (ESI) m/z 366.11 (M+H)+.

後処理

  1. customReaction mixture
  2. concentrationwas concentrated under reduced pressure
  3. dissolutionthe residue was re-dissolved in CH3CN (25 mL) to which
  4. temperatureThe reaction mixture was refluxed for 24 h
  5. customReaction mixture
  6. customReaction mixture
  7. extractionwas extracted with EtOAc (3×100 mL)
  8. washThe combined organic layer was washed with brine
  9. dry with materialdried (Na2SO4)
  10. concentrationconcentrated under reduced pressure
  11. customto afford the crude product
  12. customThe product was purified by column chromatography

出典と根拠

ORDレコード
ord-f672dcb816f04079839b6e0b97c2e4c9
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07649093B2

反応ノート

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