Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Formamide | HCID 713 | — |
| Reactant | HCID 13602723 | HCID 13602723 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22066088 | HCID 22066088 | — |
Reaction Steps
A mixture of (+/−)-2,2′,4,4′-tetrachlorobenzoin (1.0 gm, 2.9 mmol) from Step A and paraformaldehyde (0.70 gm, 24 mmol) in formamide (20 mL) was heated to 200-210° C. for 3 hr. The reaction was cooled to rt, diluted with water, and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by flash chromatography, eluting first with 10% ethyl acetate in hexanes to afford 4,5-di-(2,4-dichlorophenyl)oxazole as a higher Rf byproduct and then with 75% ethyl acetate in hexanes to elute the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572785B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-c2091b4705df4570a003cce63cdf9a6b |
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| Source note | uspto-grants-2009_08 |
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