Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19911843 | HCID 19911843 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19911844 | HCID 19911844 | — |
Reaction Steps
38.0 g (0.085 mol) of methyl 5-(2-quinolinylmethoxy)-3-(1,1,1-trifluoromethylsulphamoyl)-2-thiophenecarboxylate are dissolved in 350 ml of methanol and about 100 ml of 2N sodium hydroxide solution are added. The reaction mixture is heated under reflux and with stirring for 7 hours. The reaction solution is concentrated to 20% of its volume and diluted with 500 ml of water. The aqueous phase is extracted four times with a total of 500 ml of ether. The aqueous phase is cooled to 0° C. with stirring and acidified with 0.5N hydrochloric acid. The product precipitated in this way is filtered off with suction, digested twice with 50 ml of ice-cold ether each time and dried at 60° C./1 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05086180 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-82d112fa72d446fcbb5afd67ef0512a1 |
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| Source note | uspto-grants-1992_02 |
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