HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397364Generated: November 1, 2026
Dimethylformamide → 2-Hydroxy-4-phenylthiazole
https://huagongshe.com/reaction/1397364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Product | 2-Hydroxy-4-phenylthiazole | HCID 698903 | 75% |
Reaction Steps
A suspension of 2-bromoacetophenone (5 g, 0.0251 mol), potassium thiocyanate (8.6 g, 0.088 mol) and potassium iodide (0.25 g, 0.0015 mol) in dry DMF (25 mL) was heated to 80° C. for 2 h. The reaction mixture was concentrated to dryness under reduced pressure and the residue was dissolved in glacial acetic acid (25 mL) and 50% aqueous H2SO4 was added to it. The reaction mixture was heated to 100° C. for 10 min. The reaction mixture was poured in ice water and the precipitate formed was filtered and dried under reduced pressure to get 4-phenylthiazol-2(3H)-one (3.3 g, yield 75%) as a brown solid, which was carried through without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901156B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-747cd62c668945d9a9ceb632e061300e |
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| Source note | uspto-grants-2014_12 |
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