Thionyl Chloride → HCID 23089870、化合物

HRID 1863993ノート

反応式

HRID 1863993 の反応式
[Cl:1][C:2]1[N:10]=[CH:9][CH:8]=[C:7]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=2)[C:3]=1[C:4](O)=[O:5].S(Cl)(Cl)=O>O1CCCC1>[Cl:1][C:2]1[C:3]([CH2:4][OH:5])=[C:7]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=2)[CH:8]=[CH:9][N:10]=1

参加物

4

実験手順

To a solution of 2-chloro-4-(4-chlorophenyl)nicotinic acid (2.4 g) in tetrahydrofuran (60 ml) was added thionyl chloride (3.2 g), and the mixture was heated under reflux for 3 hrs. The solvent was evaporated under reduced pressure, and the residue was dissolved in tetrahydrofuran (60 ml). Sodium borohydride (1.5 g) was added by small portions at 0° C., and the mixture was allowed to warm gradually and stirred at room temperature for 2 hrs. Water was added to quench the reaction and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (1.9 g) as a colorless oil.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 3 hrs
  3. customThe solvent was evaporated under reduced pressure
  4. dissolutionthe residue was dissolved in tetrahydrofuran (60 ml)
  5. additionSodium borohydride (1.5 g) was added by small portions at 0° C.
  6. temperatureto warm gradually
  7. additionWater was added
  8. customto quench
  9. customthe reaction
  10. extractionthe mixture was extracted with ethyl acetate
  11. washThe organic layer was washed successively with water and saturated brine
  12. dry with materialdried over anhydrous magnesium sulfate
  13. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-07a61fb8c9714ec997527bbb5ed85889
出典データセット
uspto-grants-2009_12
特許番号
US07625887B2

反応ノート

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