HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604479Generated: October 30, 2026
Iodine → N-(5-Furan-3-yl-4-phenyl-thiazol-2-yl)-formamide
https://huagongshe.com/reaction/604479
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Furan-3-yl-1-phenyl-ethanone | HCID 57709604 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(5-Furan-3-yl-4-phenyl-thiazol-2-yl)-formamide | HCID 57709597 | — |
Reaction Steps
To a solution of 2-furan-3-yl-1-phenyl-ethanone (5.7 g, 31 mmol) and thiourea (4.7 g, 61 mmol) in DMF (57 mL) was and added iodine (7.8 g, 31 mmol). The reaction mixture was heated at 100° C. overnight, then it was diluted with water and made alkaline with saturated aqueous NH4OH, and extracted with ether. The organic phases were washed with water, dried over sodium sulfate, concentrated and purified on neutral Al2O3 using 50% ethyl acetate in hexane as eluent. Yield: 5.7 g, 69%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910613B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-d0bd42ae18bd45618907eeee605def21 |
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| Source note | uspto-grants-2011_03 |
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