Boron trifluoride → HCID 14726544、化合物

HRID 1742400

反応式

HRID 1742400 の反応式
[CH3:1][C:2]1([CH3:17])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14](Cl)=[O:15])[CH:5]=[CH:4][C:3]1=2.[CH3:18][C:19]1[CH:28]=[CH:27][C:22]([C:23](=[N:25]O)[NH2:24])=[CH:21][CH:20]=1.B(F)(F)F>O1CCOCC1>[CH3:1][C:2]1([CH3:17])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14]3[O:15][N:25]=[C:23]([C:22]4[CH:27]=[CH:28][C:19]([CH3:18])=[CH:20][CH:21]=4)[N:24]=3)[CH:5]=[CH:4][C:3]1=2

参加物

5

実験手順

8.0 g (30 millimoles) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthoyl chloride and 4.5 g (30 millimoles) of 4-methylbenzamidoxime in 250 ml of dioxane were refluxed for 1 hour. 1 ml of boron trifluoride dietherate were added and refluxing was continued for a further 4 hours. The mixture was allowed to cool, poured onto ice/water and extracted with methylene chloride. The organic phase was washed several times with water, dried over magnesium sulfate and evaporated down. The oily residue was purified by column chromatography (silica gel; n-hepatane+0.5% of ethyl acetate), and the crude product obtained from the first fractions was recrystallized from methanol to give 3.2 g of the title compound of melting point 106°-109° C.

後処理

  1. temperaturerefluxing
  2. temperatureto cool
  3. additionpoured onto ice/water
  4. extractionextracted with methylene chloride
  5. washThe organic phase was washed several times with water
  6. dry with materialdried over magnesium sulfate
  7. customevaporated down
  8. customThe oily residue was purified by column chromatography (silica gel; n-hepatane+0.5% of ethyl acetate)
  9. customthe crude product obtained from the first fractions
  10. customwas recrystallized from methanol

出典と根拠

ORDレコード
ord-24f19fe529854a7f8970175d2beaf394
出典データセット
uspto-grants-1994_08
特許番号
US05338749

関連ノート

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