D-Tartaric acid → HCID 11691408, compound
Reaction equation
[C:1]([C@H:4]([C@@H:6]([C:8]([OH:10])=[O:9])[OH:7])[OH:5])([OH:3])=[O:2].[CH:11]([N:14]([CH2:18][CH2:19][CH:20]([C:27]1[CH:32]=[C:31]([CH3:33])[CH:30]=[CH:29][C:28]=1[OH:34])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH:15]([CH3:17])[CH3:16])([CH3:13])[CH3:12].C(O)(=O)[C@H]([C@@H](C(O)=O)O)O>>[C:1]([CH:4]([CH:6]([C:8]([OH:10])=[O:9])[OH:7])[OH:5])([OH:3])=[O:2].[CH:11]([N:14]([CH2:18][CH2:19][CH:20]([C:27]1[CH:32]=[C:31]([CH3:33])[CH:30]=[CH:29][C:28]=1[OH:34])[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)[CH:15]([CH3:17])[CH3:16])([CH3:12])[CH3:13]Participants
3
Procedure
(-)-N,N-Diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropylamine hydrogen D(-)-tartrate was similarly prepared using D(-)-tartaric acid.
Sources & evidence
- ORD record
- ord-ce329c7c98d44f57ac06b5ab32f6c343
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05382600
Reaction notes
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