Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 67183740 | HCID 67183740 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59237145 | HCID 59237145 | 25% |
Reaction Steps
To an ice cold (0-5° C.) solution of ammonium hydroxide (5 mL) was added a solution of methyl 4-[(dimethylamino)diazenyl]thiophene-3-carboxylate (110 mg) in THF (2 mL) for 5 min and stirred at rt for 36 h. The solution was poured into ice cooled water and extracted with chloroform. The combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using chloroform-methanol (98:2) as eluents to give the product as a pale red color solid (25 mg, 25%), mp 168-172° C. IR (neat) νmax 3324, 3125, 2917, 2851, 1655, 1600, 1367, 1336, 1090 cm−1; 1H NMR (400 MHz, CDCl3): δ 8.55 (1H, br s), 8.19 (1H, d, J=3.6 Hz), 7.15 (1H, d, J=3.6 Hz), 5.84 (1H, br s), 3.56 (3H, br s), 3.19 (3H, br s); LC-MS (positive ion mode): m/z 199 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258119B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-8a333b08c5f24f25b312900400960658 |
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| Source note | uspto-grants-2012_09 |
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