Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-Methyl-tert-butylamine | HCID 84552 | — |
| Reactant | HCID 66836706 | HCID 66836706 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66836578 | HCID 66836578 | — |
Reaction Steps
200 mg of 1-bromo-2-chloromethyl-4,5-difluorobenzene are dissolved in 5 ml of acetonitrile. 540 mg of caesium carbonate and 206 μl of tert-butylmethylamine are added, and the mixture is stirred at 80° C. for 16 h. After cooling to 25° C., the mixture is filtered, and the filtrate is evaporated to dryness. The residue is taken up in 5 ml of ethyl acetate, the solution is washed with 5 ml of 2N sodium hydroxide solution, and the combined organic phases are dried over sodium sulfate. After filtration, the filtrate is evaporated to dryness, after which the product is isolated as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791129B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-b2e09c0116054347aa82d202f6053ed1 |
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| Source note | uspto-grants-2014_07 |
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