Aluminum(III) Chloride → HCID 14773363, compound
Reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:11][O:12][C:13]1[CH:29]=[CH:28][C:16]([C:17]([C:19]2[CH:20]=[C:21]([S:24]([NH2:27])(=[O:26])=[O:25])[S:22][CH:23]=2)=O)=[CH:15][CH:14]=1>C1COCC1>[CH3:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:17][C:19]2[CH:20]=[C:21]([S:24]([NH2:27])(=[O:26])=[O:25])[S:22][CH:23]=2)=[CH:28][CH:29]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a solution of 0.667 g (0.005 mol) aluminum chloride in 10 ml THF at 0°-10° C. was added a solution of 0.19 g (0.005 mol) lithium aluminum hydride in 10 ml THF dropwise. Then, a solution of 0.6 g (0.002 mol) 4-(4-methoxybenzoyl)thiophene-2-sulfonamide in 10 ml THF was added dropwise and the resulting mixture was heated at 60° C. overnight at which time all starting material was consumed. The cooled reaction mixture was quenched with saturated aqueous sodium potassium tartrate solution and the resulting grey solid was filtered off. The filtrate was dried and the solvent evaporated to give the title compound.
Workup
- customwas consumed
- customThe cooled reaction mixture
- customwas quenched with saturated aqueous sodium potassium tartrate solution
- filtrationthe resulting grey solid was filtered off
- customThe filtrate was dried
- customthe solvent evaporated
Sources & evidence
- ORD record
- ord-2ef4ad623f584f46a5f885caa4c3fcfe
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04914111
Reaction notes
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