Citric Acid → HCID 19031546, compound
Reaction equation
[C:1]([OH:13])(=[O:12])[CH2:2][C:3]([CH2:8][C:9]([OH:11])=[O:10])([C:5]([OH:7])=[O:6])[OH:4].[Cl:14][C:15]1[CH:16]=[C:17]([C:22]2([CH:26]([OH:35])[CH2:27][S:28][CH2:29][CH2:30][CH2:31][N:32]([CH3:34])[CH3:33])[CH2:25][CH2:24][CH2:23]2)[CH:18]=[CH:19][C:20]=1[Cl:21]>C(O)C.CCOCC>[C:1]([OH:13])(=[O:12])[CH2:2][C:3]([CH2:8][C:9]([OH:11])=[O:10])([C:5]([OH:7])=[O:6])[OH:4].[Cl:14][C:15]1[CH:16]=[C:17]([C:22]2([CH:26]([OH:35])[CH2:27][S:28][CH2:29][CH2:30][CH2:31][N:32]([CH3:34])[CH3:33])[CH2:25][CH2:24][CH2:23]2)[CH:18]=[CH:19][C:20]=1[Cl:21]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of citric acid (1.77 g) in hot ethanol (10 ml) was added to a solution of (-) -1-[1-(3,4-dichlorophenyl)cyclobutyl]-2-[3-(dimethylamino)-propylthio]ethanol (3.42 g) in ether (30 ml), and the mixture was stored at 4° C. for 18 hours. The resulting solid was collected by filtration, washed with ether and dried in vacuo at ambient temperature for 24 hours, to give (-)-1-[1-(3,4-dichlorophenyl)cyclobutyl]-2-[3-(dimethylamino)propylthio]ethanol citrate as a white solid (3.9 g) , m.p. 109°-115° C., [α]rtD =-10.17° (C=1; methanol) .
Workup
- filtrationThe resulting solid was collected by filtration
- washwashed with ether
- customdried in vacuo at ambient temperature for 24 hours
Sources & evidence
- ORD record
- ord-ca8e6396791342f4b85d11c4b3282623
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05652271
Reaction notes
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