Hydrochloric Acid → 6-(4-Chloro-1-butenyl)-3,4-dihydrocarbostyril

HRID 2291159Notes

Reaction equation

HRID 2291159 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH2:11][CH2:10]2)=O.[BH4-].[Na+].Cl>CO>[Cl:1][CH2:2][CH2:3][CH:4]=[CH:5][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH2:11][CH2:10]2

Participants

5

Procedure

4.0 Grams of 6-(4-chloro-1-oxobutyl)-3,4-dihydrocarbostyril was disposed in 200 ml of methanol, and the suspension was stirred at a room temperature. Then 2.0 g of sodium borohydride was added to the suspension gradually and the reaction was continued for 1 hour. Next, 3 ml of concentrated hydrochloric acid was added to the reaction mixture and the mixture was concentrated under a reduce pressure with heat-refluxing condition to obtain a residue. The residue was extracted with chloroform and the chloroform layer was washed with water and dried. Then coloroform was removed by distillation under a reduced pressure to obtain a residue, and the residue was recrystallized from ethanol to obtain 2.4 g of 6-(4-chloro-1-butenyl)-3,4-dihydrocarbostyril in yellow needle-like crystals. Melting point: 153°-155° C.

Workup

  1. concentrationthe mixture was concentrated under a reduce pressure
  2. temperaturewith heat-refluxing condition
  3. customto obtain a residue
  4. extractionThe residue was extracted with chloroform
  5. washthe chloroform layer was washed with water
  6. customdried
  7. customThen coloroform was removed by distillation under a reduced pressure
  8. customto obtain a residue
  9. customthe residue was recrystallized from ethanol

Sources & evidence

ORD record
ord-dbb10ee2b22443b39fb48f1caf9c3156
Source dataset
uspto-grants-1986_10
Patent number
US04619932

Reaction notes

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