Diethylamine → 2-Butene-1,4-diamine, N1,N1,N4,N4-tetraethyl-, (2E)-
Reaction equation
[CH2:1]([NH:3][CH2:4][CH3:5])[CH3:2].Br[CH2:7]/[CH:8]=[CH:9]/[CH2:10]Br>C1(C)C=CC=CC=1>[CH2:1]([N:3]([CH2:4][CH3:5])[CH2:7]/[CH:8]=[CH:9]/[CH2:10][N:3]([CH2:4][CH3:5])[CH2:1][CH3:2])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Diethylamine (1.5 g, 20 mmol) in toluene (50 ml) was added to a stirred solution of (E)-1,4-dibromobut-2-ene (2.14 g, 10 mmol) in toluene (50 ml) at room temperature, and the solution was stirred for 4 h. The white precipitate formed was filtered off, washed with ether (2×20 ml), and dissolved in hot aqueous ethanol. The solution was allowed to cool and acetone was added. The white precipitate formed was filtered off and washed with acetone to yield (E)-N,N,N',N'-tetraethyl-1,4-diaminobut-2-ene (TED) dihydrobromide (2.16 g, 60%). δH (90 MHz, D2O) 1.10 (12H, t), 3.15 (8H, q), 3.98 (4H, m) and 5.90 (2H, m).
Workup
- customThe white precipitate formed
- filtrationwas filtered off
- washwashed with ether (2×20 ml)
- dissolutiondissolved in hot aqueous ethanol
- temperatureto cool
- additionacetone was added
- customThe white precipitate formed
- filtrationwas filtered off
- washwashed with acetone
Sources & evidence
- ORD record
- ord-1fb48e9f2c5544c0ad1d3112c21c6b66
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05599847
Reaction notes
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