Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium chlorodifluoroacetate | HCID 2734985 | — |
| Reactant | HCID 178470300 | HCID 178470300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 117819052 | HCID 117819052 | — |
Reaction Steps
In a round bottom flask (5 litre) was taken Ethyl 6-hydroxy-5-methylpyrimidine-4-carboxylate 40 (85 g, 466 mmol), chlorodifluoroacetic acid sodium salt (106.7 g, 699 mmol), sodium carbonate (98.9 g, 933 mmol), acetonitrile (1500 ml) and DMF (425 ml). The reaction mixture was heated to 90° C. for 16 h. The Progress of the reaction was monitored by LCMS. The reaction mixture was cooled to room temperature and then neutralized with saturated ammonium chloride. The solvent was removed under vacuum and extracted with ethyl acetate. The combined organic layer was washed with water, brine and concentrated under reduced pressure. The crude compound was purified through silica gel chromatography eluting (3-4% ethyl acetate) to afford ethyl 6-(difluoromethoxy)-5-methylpyrimidine-4-carboxylate 48b as a pale yellow liquid. Yield: 14 g (13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163020B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-246e2201b73448b9bf8b9bdf0c601aad |
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| Source note | uspto-grants-2015_10 |
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