Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12038723 | HCID 12038723 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10943925 | HCID 10943925 | 74.5% |
Reaction Steps
To a solution of 3.00 g (12.18 mM) of ethyl 5-thia-1,8b-diazaacenaphthylene-4-carboxylate in methanol (9 ml) was added 18 ml (18 mM) of 1N-aqueous solution of sodium hydroxide at room temperature and the mixture was stirred for 2.5 hours. This reaction mixture was cooled to 0° C. and 1N-hydrochloric acid was added until the pH had been brought to 5. The resulting crystals were harvested by filtration. This crystal crop was rinsed with water, ethanol and diethyl ether to provide the title compound as orange-colored solid (yield 1.98 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235731B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-d24f409ea2bf4afaa7e096acc9f224cf |
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| Source note | uspto-grants-2001_05 |
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