Dimethylformamide → HCID 23452135, compound
Reaction equation
[C:1]1(=[O:11])[NH:5][C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[K].CN(C)[CH:15]=[O:16]>>[O:16]1[CH:15]=[CH:1][CH:2]=[C:10]1[CH2:9][CH2:8][CH2:7][CH2:3][N:5]1[C:1](=[O:11])[C:2]2[C:3](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4]1=[O:6]Participants
3
Procedure
2[1-(4-bromobutyl)]furan (406 mg) and potassium phthalimide (370 mg) were stirred together at room temperature in dry dimethylformamide overnight. The solution was poured into ice-water and the resulting white solid filtered, dried and recrystallised from chloroform/petroleum ether (b.p. 60°-80°) to give 2-[4-(2-Furanyl)butyl]-1H-isoindole-1,3(2H)-dione as white microcrystals (430 mg) m.p. 61°-63°.
Workup
- filtrationthe resulting white solid filtered
- customdried
- customrecrystallised from chloroform/petroleum ether (b.p. 60°-80°)
Sources & evidence
- ORD record
- ord-3a11d5aa0a214a5ca7fbbc4fb29ac07c
- Source dataset
- uspto-grants-1979_10
- Patent number
- US04169855
Reaction notes
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