HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 2-Amino-4-Phenylthiazole-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Bromo-3-oxo-3-phenylpropanenitrile | HCID 11961596 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-4-Phenylthiazole-5-carbonitrile | HCID 21455552 | — |
Reaction Steps
2-Bromo-3-oxo-3-phenylpropionitrile (0.5 g, 3.4 mmol) was mixed with thiourea (0.52 g, 6.8 mmol) and iodine (0.43 g, 3.4 mmol) and the mixture was heated on a steam bath for 12 h. It was then diluted with water and made alkaline with saturated aqueous NH4OH, and extracted with ethyl acetate. The organic phases were washed with water and brine, dried over sodium sulfate, and evaporated to dryness to give the crude product, which was used in the next reaction without any further purification. Yield: 0.2 g, 29%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910613B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-03d78c88d23b42f9abb204f8b42379f8 |
| Source note | uspto-grants-2011_03 |