Ethylenediamine → HCID 518891, compound
Reaction equation
[CH:1](=O)[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[CH2:10]([NH2:13])[CH2:11][NH2:12]>C(O)C>[CH:1](=[N:12][CH:11]=[CH:10][N:13]=[CH:1][C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Salicylaldehyde (3.9 g; 32 mmol) and ethylenediamine (1.0 g; 16 mmol) were added to 40 mL ethanol in a 100-mL one-necked flask. The mixture was stirred for 3 hours at room temperature. The formed precipitate was filtered off with a Büchner funnel. The precipitate was washed three times with 20 mL methanol. The solids were collected and dried overnight at 40° C. under vacuum. The intermediate ligand N,N′-bis(salicylidene)-1,2-diaminoethylene was obtained as a yellow solid with a yield of 80.5% (3.62 g; 13.5 mmol).
Workup
- filtrationThe formed precipitate was filtered off with a Büchner funnel
- washThe precipitate was washed three times with 20 mL methanol
- customThe solids were collected
- customdried overnight at 40° C. under vacuum
Sources & evidence
- ORD record
- ord-67fc75743e174f9f950e49e93a36ed5e
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933190B2
Reaction notes
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