Sodium Bicarbonate → HCID 22759449, compound
Reaction equation
Br.[Br:2][CH2:3][CH2:4][NH:5][C:6]1[CH2:10][CH:9]([C:11]2[C:16]([Cl:17])=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:18])[CH2:8][N:7]=1.C(=O)(O)[O-].[Na+]>C(O)(C)C>[BrH:2].[Cl:18][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]([Cl:17])[C:11]=1[CH:9]1[CH2:8][N:7]2[CH2:3][CH2:4][N:5]=[C:6]2[CH2:10]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred mixture of 2-β-bromoethylamino-4-(2,6-dichlorophenyl)-1-pyrroline hydrobromide (46.35 g.), anhydrous sodium bicarbonate (9.3 g.) and dry isopropanol (350 ml.) is heated under reflux for 4 hours with exclusion of moisture, the hot mixture is filtered and the solid residue is stirred and heated under reflux with dry isopropanol (350 ml.) for 1 hour. The hot mixture is filtered and the combined isopropanol filtrates are evaporated to dryness under reduced pressure. The residue is dissolved in boiling ethanol (200 ml.) and the solution is concentrated to 125 ml. and allowed to cool. The mixture is filtered and there is thus obtained as solid residue 6-(2,6-dichlorophenyl)-2,3,6,7-tetrahydro-5H-pyrrolo[1,2-a]imidazole hydrobromide, m.p. 297°-299° C.
Workup
- temperatureis heated
- temperatureunder reflux for 4 hours with exclusion of moisture
- filtrationthe hot mixture is filtered
- temperatureheated
- temperatureunder reflux with dry isopropanol (350 ml.) for 1 hour
- filtrationThe hot mixture is filtered
- customthe combined isopropanol filtrates are evaporated to dryness under reduced pressure
- dissolutionThe residue is dissolved
- concentrationthe solution is concentrated to 125 ml
- temperatureto cool
- filtrationThe mixture is filtered
Sources & evidence
- ORD record
- ord-8dcd6d1af41c49b2986384f52598e8b5
- Source dataset
- uspto-grants-1978_11
- Patent number
- US04126685
Reaction notes
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