Toluene → HCID 86595355, compound
Reaction equation
[Cl:1][CH2:2][CH:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=1.C[C:18]1[NH:19][CH:20]=[CH:21][N:22]=1.[C:23]1(C)C=CC=CC=1>>[Cl-:1].[CH3:23][N+:22]1[CH:21]=[CH:20][N:19]([CH2:2][CH:3]2[CH2:7][CH2:6][CH2:5][N:4]2[C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=2)[CH:18]=1Participants
4
Procedure
16.8 g (0.07 mol) of 2-chloromethyl-1-(4-nitrophenyl)pyrrolidine (1), 17.2 g (0.21 mol) of methylimidazole and 70 ml of toluene were refluxed for 9 hours. The solvent was evaporated off and the product was recrystallized from isopropanol and then dried under vacuum. 3 g of yellow crystals (2) were obtained.
Workup
- customThe solvent was evaporated off
- customthe product was recrystallized from isopropanol
- customdried under vacuum
Sources & evidence
- ORD record
- ord-638fa5ddce4e489ea4fa24a0c49d2e8e
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07132543B2
Reaction notes
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