Hydrochloric Acid → HCID 69677733, compound
Reaction equation
C([N:4]([C:10]1[CH:15]=[CH:14][C:13]([CH3:16])=[C:12]([CH3:17])[CH:11]=1)[C@@H:5]([C:7]([OH:9])=[O:8])[CH3:6])(=O)C.[ClH:18]>C(O)(=O)C>[ClH:18].[CH3:17][C:12]1[CH:11]=[C:10]([NH:4][C@@H:5]([C:7]([OH:9])=[O:8])[CH3:6])[CH:15]=[CH:14][C:13]=1[CH3:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of N-acetyl-3,4-dimethylphenyl-D-alanine (5.0 g) in a mixture of concentrated hydrochloric acid (50 ml) and acetic acid (50 ml) was stirred under reflux for 20 hours. After being cooled to room temperature, the resulting precipitates were collected by filtration and washed with ethyl acetate to give colorless crystals of 3,4-dimethylphenyl-D-alanine hydrochloride (3.75 g).
Workup
- temperatureunder reflux for 20 hours
- customthe resulting precipitates
- filtrationwere collected by filtration
- washwashed with ethyl acetate
Sources & evidence
- ORD record
- ord-bb7b2290d4244cb09d367f8f0cbc1ddf
- Source dataset
- uspto-grants-2005_08
- Patent number
- US06924278B2
Reaction notes
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