Carbon Disulfide → HCID 86098808, compound
Reaction equation
[NH2:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[CH2:4][NH:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][CH3:14].[C:19](=S)=[S:20]>C(O)C>[CH3:14][O:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[CH2:6][N:5]1[CH2:4][C:3]2[C:2](=[CH:18][CH:17]=[CH:16][CH:15]=2)[NH:1][C:19]1=[S:20]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.0 g (16.51 mmol) (2-aminobenzyl)(2-methoxybenzyl)amine in 100 mL ethanol was mixed with 40 mL CS2 and heated at reflux for 8 hours, forming a yellow precipitate. The mixture was evaluated and the resulting solids were recrystallized in ethanol; 4.24 g white solids.
Workup
- temperatureheated
- temperatureat reflux for 8 hours
- customforming a yellow precipitate
- customthe resulting solids were recrystallized in ethanol
Sources & evidence
- ORD record
- ord-cc12999b4ee548b88ba58166bc43f9b2
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686002B2
Reaction notes
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