Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12151356 | HCID 12151356 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12151353 | HCID 12151353 | 70.3% |
Reaction Steps
8.3 g (0.031 mol) of [1-(4-diethoxymethylpyrimidin-5-yl)-2-methylpropyl]methylamine and 6.4 g (46 mmol) of potassium carbonate were added to 100 ml of acetonitrile, and then 5.8 g (0.038 mol) of phenylacetyl chloride was dropwise added at room temperature and reacted for 2 hours. After completion of the reaction, the product was poured into water and extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution, water and an aqueous sodium chloride solution in this order, dried and concentrated, and the obtained oily product was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:5 to ethyl acetate), to obtain 8.4 g (yield: 70%) of N-[1-(4-diethoxymethylpyrimidin-5-yl)-2-methylpropyl]-N-methyl-2-phenyl acetamide as colorless viscous liquid (nD2=1.5253)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806230B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-c671939eaf8c42acaa2cb19b5fa7318f |
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| Source note | uspto-grants-2004_10 |
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