Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86646883 | HCID 86646883 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 49783916 | HCID 49783916 | 45% |
Reaction Steps
To a solution of ethyl 3-[(dimethylamino)diazenyl]-5-(tert-butyl)selenophene-2-carboxylate (400 mg, 1.2 mmol) prepared as described in Example 4 step c) in methanol (10 mL) was added a solution of sodium hydroxide (240 mg, 6.04 mmol) in water (5 mL) and stirred at room temperature (rt) for 16 h. The mixture was diluted with ice cold water and acidified with dil. HCl. The mixture was stirred for 30 min and the precipitated solid was filtered, washed with water and dried. The product was recrystallized from hexane-chloroform to give the product as a pale brown color solid (160 mg, 45%), mp 120-122° C. IR (neat) νmax 2960, 2927, 1713, 1248, 1180, 1110, 1069, 1010, 844, 767 cm−1; 1H NMR (400 MHz, CDCl3): δ 12.23 (1H, s, —COOH), 7.38 (1H, s, H-4), 3.63 (3H, s, —NCH3), 3.23 (3H, s, —NCH3), 1.39 (9H, s, 3×—CH3); 13C NMR (100 MHz, CDCl3): δ 171.7, 164.1, 153.7, 123.2, 115.6, 44.2, 37.2, 36.9, 32.4; LC-MS (positive ion mode): m/z 324, 326 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143237B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-d79c6afc77304ec5b644b619d9628ad5 |
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| Source note | uspto-grants-2012_03 |
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