Hydrochloric Acid → HCID 71073521, compound
Reaction equation
[NH2:1][C@H:2]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[Cl:14])[CH2:3][C:4]([OH:6])=[O:5].Cl.[CH3:16][CH2:17]O>>[CH2:16]([O:5][C:4](=[O:6])[CH2:3][C@H:2]([NH2:1])[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[Cl:14])[CH3:17]Participants
4
Procedure
(R)-3-Amino-4-(2-chloro-phenyl)-butyric acid (10 g, 50 mmol) was dissolved in absolute EtOH (250 mL). Concentrated HCl (2 mL) was added and the mixture was heated to reflux overnight. The product was vacuumed to dryness and azeotroped with toluene (4×50 mL), then placed under high vacuum overnight to yield the title compound as a white solid (10 g).
Workup
- temperaturethe mixture was heated
- temperatureto reflux overnight
- customazeotroped with toluene (4×50 mL)
- customplaced under high vacuum overnight
Sources & evidence
- ORD record
- ord-dd6c8db43d3e46e987dd52c7bf6e86d5
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513244B2
Reaction notes
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