| Identification | Back Directory | [Name]
DIBENZYLIDENE ETHYLENEDIAMINE | [CAS]
104-71-2 | [Synonyms]
DIBENZYLIDENE ETHYLENEDIAMINE
N,N'-dibenzylideneethylenediamine
N,N'-Ethylenebisbenzenemethanimine
N,N'-Dibenzylidene-1,2-ethanediamine
N,N'-Dibenzylideneethane-1,2-diamine
N,N'-BIS(BENZYLIDENE)ETHYLENEDIAMINE
Ethylenediamine, N,N'-dibenzylidene-
N1,N2-Dibenzylideneethane-1,2-diaMine
n,n’-bis(phenylmethylene)-2-ethanediamine
N,N'-Bis(phenylmethylene)-1,2-ethanediamine
N,N'-BIS(PHENYLMETHYLENE)-1,2-ETHYLENEDIAMINE
1,2-Ethanediamine, N,N'-bis(phenylmethylene)-
N,N'-Bis(phenylmethylene)-1,2-ethylenediamine, 99.5+% | [EINECS(EC#)]
203-229-6 | [Molecular Formula]
C16H16N2 | [MDL Number]
MFCD00022040 | [MOL File]
104-71-2.mol | [Molecular Weight]
236.31 |
| Hazard Information | Back Directory | [Chemical Properties]
light yellow to yellow crystalline powder | [Synthesis]
GENERAL METHOD: Benzaldehyde (60 mmol) was added slowly and dropwise to a methanol (80 mL) solution of ethylenediamine (100 mmol) at 0°C. Subsequently, the reaction mixture was stirred at room temperature for 12 h (Scheme 1) [4]. Upon completion of the reaction, the crude product N1,N2-dibenzylidene ethyl-1,2-diamine was vacuum filtrated. The obtained residue was dissolved in 100 mL of dichloromethane and dried with anhydrous potassium carbonate. Finally, the solvent was evaporated under high vacuum to obtain pure N1,N2-dibenzylidene ethyl-1,2-diamine. | [References]
[1] Journal of the American Chemical Society, 1998, vol. 120, # 51, p. 13370 - 13382
[2] Tetrahedron Letters, 1998, vol. 39, # 47, p. 8645 - 8646
[3] Synthetic Communications, 2003, vol. 33, # 18, p. 3193 - 3204
[4] Synthesis, 1980, # 4, p. 303 - 305
[5] Bulletin of the Chemical Society of Ethiopia, 2014, vol. 28, # 1, p. 73 - 79 |
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