Hydrochloric Acid → HCID 54104191, compound
Reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[Cl:5][CH2:6][C:7](Cl)=[O:8].[C:10]1([CH3:29])[CH:15]=[CH:14][C:13]([S:16]([NH:19][CH:20]2[CH2:28][C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH2:21]2)(=[O:18])=[O:17])=[CH:12][CH:11]=1.Cl>C(Cl)CCl>[Cl:5][CH2:6][C:7]([C:24]1[CH:23]=[C:22]2[C:27](=[CH:26][CH:25]=1)[CH2:28][CH:20]([NH:19][S:16]([C:13]1[CH:12]=[CH:11][C:10]([CH3:29])=[CH:15][CH:14]=1)(=[O:17])=[O:18])[CH2:21]2)=[O:8]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
25.4 g (0.19 mol) of anhydrous aluminium chloride are suspended in 80 ml of ethylene chloride and 11.1 g (0.095 mol) of chloroacetyl chloride are added. 22.8 g (0.079 mol) of 2-p-toluenesulphonamido-indane are then added and the mixture is stirred for 2 hours at room temperature. The product is then decomposed by means of ice and hydrochloric acid and the reaction product is isolated from the organic phase and recrystallised from ethyl acetate/cyclohexane.
Workup
- customthe reaction product is isolated from the organic phase
- customrecrystallised from ethyl acetate/cyclohexane
Sources & evidence
- ORD record
- ord-363262bdc9524783b2a45cbe5e394b24
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04929754
Reaction notes
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