Hydrochloric Acid → Ethyl 3-amino-3-(3-nitrophenyl)propanoate hydrochloride
Reaction equation
[ClH:1].[NH2:2][CH:3]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-:16])=[O:15])[CH:9]=1)[CH2:4][C:5]([OH:7])=[O:6].Cl.[CH2:18](O)[CH3:19]>>[ClH:1].[NH2:2][CH:3]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-:16])=[O:15])[CH:9]=1)[CH2:4][C:5]([O:7][CH2:18][CH3:19])=[O:6]Participants
4
Procedure
60 g of (1a) were suspended in 660 ml of ethanol, and gaseous HCl was passed in for 1 h. The reaction mixture was then heated under reflux for 4 h and then cooled and concentrated. 62 g of a white solid were obtained.
Workup
- customwas passed in for 1 h
- temperatureThe reaction mixture was then heated
- temperatureunder reflux for 4 h
- temperaturecooled
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-bc088d423f3b4394927a13bad3b6a3ba
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06589972B2
Reaction notes
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