1-Bromo-3-chloropropane → HCID 10658563, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH2:5][CH2:6][C:7](=[O:13])[NH:8]2.[H-].[Na+].[Na].Br[CH2:18][CH2:19][CH2:20][Cl:21]>CN(C)C=O>[Cl:21][CH2:20][CH2:19][CH2:18][N:8]1[C:9]2[C:4](=[C:3]([O:2][CH3:1])[CH:12]=[CH:11][CH:10]=2)[CH2:5][CH2:6][C:7]1=[O:13]Participants
Procedure
To a solution of 5-methoxy-3,4-dihydrocarbostyril (53.1 g, 0.3 mole) in 200 ml of dimethylformamide (DMF) was added portionwise 60% sodium hydride in oil (19.2 g, 0.4 mole) at room temperature, and the mixture was stirred for 30 minutes. To the thus-obtained solution of the sodium salt of 5-methoxy-3,4-dihydrocarbostyril in DMF was added 1-bromo-3-chloropropane (94 ml, 0.6 mole). The mixture was stirred at 80°-90° C. for 8 hours. The DMF was distilled off under reduced pressure, and the residue was extracted with chloroform. The extract was washed with water and dried (anhydrous magnesium sulfate), the chloroform was distilled off under reduced pressure, and the residue was recrystallized from ethanol to give 59 g of 1-(3-chloropropyl)-5-methoxy-3,4-dihydrocarbostyril as colorless needles.
Workup
- stirringThe mixture was stirred at 80°-90° C. for 8 hours
- distillationThe DMF was distilled off under reduced pressure
- extractionthe residue was extracted with chloroform
- washThe extract was washed with water
- dry with materialdried (anhydrous magnesium sulfate)
- distillationthe chloroform was distilled off under reduced pressure
- customthe residue was recrystallized from ethanol
Sources & evidence
- ORD record
- ord-974446ebb44544228b78da43d82be874
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05556857
Reaction notes
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