Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21838739 | HCID 21838739 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21838732 | HCID 21838732 | — |
Reaction Steps
92 ml of a 10% ethanolic potassium hydroxide solution are added to a solution of 31.4 g (0.101 mol) of methyl 3-[(ethoxycarbonyl)amino]-6-methoxybenzo[b]thiophene-2-carboxylate in 230 ml of ethanol. The mixture is heated at 60° C. for 10 minutes and is then poured onto ice-cold water. The mixture is acidified by addition of a 6N hydrochloric acid solution and the precipitate formed is filtered off, rinsed with water and dried under reduced pressure. The solid is triturated in ethanol. 22.8 g of product are recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05969146 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-b3acc13d3c1749f19660bfefccba2738 |
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| Source note | uspto-grants-1999_10 |
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