Ammonium Hydroxide → HCID 18948387, compound
Reaction equation
[OH-].[NH4+:2].[O:3]1[CH2:8][CH2:7][N:6]([CH:9]([CH3:15])[C:10](OCC)=[O:11])[CH2:5][CH2:4]1>CO>[O:3]1[CH2:8][CH2:7][N:6]([CH:9]([CH3:15])[C:10]([NH2:2])=[O:11])[CH2:5][CH2:4]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3.5 g (40 mmole) of morpholine were added to a mixture of 3.6 g (20 mmole) of ethyl 2-bromopropionate and 50 ml of dry benzene, and then the mixture was heated under reflux for 7 hours. At the end of this time, the reaction mixture was filtered, the filtrate was concentrated by evaporation under reduced pressure, and the residue was dissolved in chloroform. The resulting solution was washed with water, dried, and concentrated by evaporation under reduced pressure, to give 3.19 g of ethyl 2-morpholinopropionate. 10 ml of methanol and 10 ml of a concentrated aqueous solution of ammonium hydroxide were then added to 3.1 g (16.6 mmole) of this ethyl 2-morpholinopropionate, and the resulting mixture was heated under reflux for 28 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and the residue was dried by heating it under reduced pressure, to give 2-morpholinopropionamide as a precipitate.
Workup
- temperaturethe resulting mixture was heated
- temperatureunder reflux for 28 hours
- concentrationAt the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure
- customthe residue was dried
- temperatureby heating it under reduced pressure
Sources & evidence
- ORD record
- ord-e59961d9c41b42b69f24e318e88e4f13
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05378690
Reaction notes
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