Benzoylacetone → HCID 67906974, compound
Reaction equation
[C:1]([CH2:9][C:10](=O)[CH3:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N:13]1([CH2:19][CH2:20][NH2:21])[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>C1(C)C=CC=CC=1>[N:13]1([CH2:19][CH2:20][NH:21][C:10]([CH3:11])=[CH:9][C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 28.7 g. (0.177 mole) of benzoylacetone and 23.2 ml. (0.177 mole) of 2-(4-morpholinyl)ethylamine in 600 ml. of toluene was heated under reflux for ten and a half hours under a Dean-Stark trap and the solution then cooled and taken to dryness to give N-[2-(4-morpholinyl)ethyl]-N-(1-methyl-3-oxo-3-phenylpropenyl)amine as a yellow solid.
Workup
- temperatureunder reflux for ten and a half hours under a Dean-Stark trap
- temperaturethe solution then cooled
Sources & evidence
- ORD record
- ord-86f7c5308fda4e5c8a236718c50fec7b
- Source dataset
- uspto-grants-1988_10
- Patent number
- USRE032761
Reaction notes
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