Propionic Acid → HCID 70546288, compound
Reaction equation
[NH2:1][CH2:2][CH:3]([OH:29])[CH2:4][NH:5][CH:6]([CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([CH:26]([CH3:28])[CH3:27])=[CH:22][CH:21]=1)[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([CH:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=1.[C:30]([OH:34])(=[O:33])[CH2:31][CH3:32]>CCOCC>[C:30]([OH:34])(=[O:33])[CH2:31][CH3:32].[C:30]([OH:34])(=[O:33])[CH2:31][CH3:32].[NH2:1][CH2:2][CH:3]([OH:29])[CH2:4][NH:5][CH:6]([CH2:18][CH2:19][C:20]1[CH:21]=[CH:22][C:23]([CH:26]([CH3:28])[CH3:27])=[CH:24][CH:25]=1)[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([CH:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 1-amino-3-{{3-[4-(1-methylethyl)phenyl]-1-{2-[4-(1-methylethyl)phenyl]ethyl}propyl}amino]-2-propanol (3.97 g., 0.01 m.) in anhydrous ether (ca. 50 ml.) is added dropwise over ca. 10 minutes a mixture of propionic acid (1.49 g., 0.02 m.) and ether (10 ml.). The resultant mixture is allowed to stir at ambient temperature for several hours, and the ether then removed in vacuo to yield 1-amino-3-{{3-[4-(1-methylethyl)-phenyl]-1-{2-[4-(1-methylethyl)phenyl]ethyl}propyl}amino]-2-propanol dipropionate.
Workup
- customthe ether then removed in vacuo
Sources & evidence
- ORD record
- ord-c7db4af150cf4863b4fb07e2184f11a7
- Source dataset
- uspto-grants-1982_01
- Patent number
- US04311709
Reaction notes
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