Calcium Hydroxide → HCID 86755942, compound
Reaction equation
[OH-].[Ca+2:2].[OH-].[Cl:4][C:5]1[CH:34]=[CH:33][C:8]([O:9][CH:10]([CH3:32])[CH2:11][O:12][N:13]=[C:14]([CH:18]2[C:23](=[O:24])[CH2:22][CH:21]([CH:25]3[CH2:30][CH2:29][CH2:28][S:27][CH2:26]3)[CH2:20][C:19]2=[O:31])[CH2:15][CH2:16][CH3:17])=[CH:7][CH:6]=1>CO>[Ca:2].[Cl:4][C:5]1[CH:34]=[CH:33][C:8]([O:9][CH:10]([CH3:32])[CH2:11][O:12][N:13]=[C:14]([CH:18]2[C:23](=[O:24])[CH2:22][CH:21]([CH:25]3[CH2:30][CH2:29][CH2:28][S:27][CH2:26]3)[CH2:20][C:19]2=[O:31])[CH2:15][CH2:16][CH3:17])=[CH:7][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of calcium hydroxide (0.2 g) in 30 ml of methanol was added to a solution of 2-{1-[2-(4-chlorophenoxy)propyloximino]butyl}-5-tetrahydrothiopyran-3-ylcyclohexane-1,3-dione (2.5 g) in 80 ml of methanol with vigorous stirring. The mixture was subsequently stirred for 5 hours at room temperature, whereupon the solvent was removed in vacuo. Yield: 2.6 g of calcium salt.
Workup
- customwas removed in vacuo
Sources & evidence
- ORD record
- ord-e1ef4ca0a13945dfb7ed1455a4da72de
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06133202
Reaction notes
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