Acetone → HCID 12906590, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:14](=[O:15])[CH:13]2[CH2:16][CH2:17][CH2:18][C:11](=[CH:12]2)C1=O.[CH:20]([NH2:23])([CH3:22])[CH3:21].C[C:25](C)=[O:26]>>[CH:20]([NH:23][C:25](=[O:26])[C:16]1[CH2:17][CH2:18][CH2:11][CH2:12][C:13]=1[C:14]([NH:9][C:3]1[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=1[F:1])=[O:15])([CH3:22])[CH3:21]Participants
4
Procedure
In acetone (40 ml) was dissolved N-(2-fluoro-4-chlorophenyl)-3,4,5,6-tetrahydroisophthalimide (2.8 g) and while stirring at room temperature, isopropylamine (0.6 g) was added. The mixture was allowed to stand for 10 hours, after which time the precipitate was recovered by filtration and washed with acetone. Yield 3.0 g.; m.p. 188°-189° C.
Workup
- filtrationafter which time the precipitate was recovered by filtration
- washwashed with acetone
Sources & evidence
- ORD record
- ord-973737407e93412f8535932eb45883a4
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04328367
Reaction notes
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