Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 2'-Fluoro-4'-hydroxyacetophenone | HCID 2724912 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67072133 | HCID 67072133 | 79.9% |
Reaction Steps
A suspension of 12.0 g (77.9 mmol) of 2-fluoro-4-hydroxyacetophenone, 27.9 g (85.6 mmol) of cesium carbonate and 11.6 ml (77.9 mmol) of ethyl 2-bromo-2-methylpropionate in 200 ml of DMF was heated at 50° C. for 3 days. Twice a day additional 12.7 g (38.9 mmol) of cesium carbonate and 5.8 ml (38.9 mmol) of ethyl 2-bromo-2-methylpropionate were added (total of 2.5 equivalent). The mixture was neutralized with aqueous 10% KHSO4 and extracted with ether (3×). The organic phases were washed with aqueous 10% KHSO4, aqueous 10% NaCl and dried over sodium sulfate. The crude product was purified by flash chromatography over silica gel with heptane/AcOEt 9:1 to 6:1, to give 16.7 g of the title compound as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115611B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-d337037cf8f149b4b5c3bb1cf0bc043e |
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| Source note | uspto-grants-2006_10 |
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