関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6-methoxy-N-methylpyridin-2-amine | HCID 7019168 | — |
| 反応物 | 4-(Trifluoromethyl)phenyl carbonochloridate | HCID 15917597 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 4-trifluoromethylphenyl N-(6-methoxy-2-pyridyl)-N-methylcarbamate | HCID 13387577 | 62% |
反応手順
To the mixture of 1.38 g of 2-methoxy-6-methylaminopyridine and 1.38 g of anhydrous potassium carbonate in 20 ml of acetone was added dropwise the solution of 2.25 g of 4-trifluoromethylphenyl chloroformate in 20 ml of acetone under stirring at room temperature. The mixture was stirred for 30 minutes and then was refluxed for 2 hours. After the reaction mixture was cooled to room temperature, it was poured into water and the product was extracted with benzene. The benzene solution, successively washed with water and brine, was dried over anhydrous magnesium sulfate. The residue obtained by the removal of benzene under reduced pressure was chromatographed through silica gel column using benzene as an eluent to give 2.02 g of pure 4-trifluoromethylphenyl N-(6-methoxy-2-pyridyl)-N-methylcarbamate as solid in the yield of 62%. A part of the solid was recrystallized from hexane and crystalls having melting point of 85° to 86° C. were obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04554012 |
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| 出典データセット | uspto-grants-1985_11 |
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| ORD ID | ord-baa0b19a408d4b28a849a04cd0e9275f |
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| 出典メモ | uspto-grants-1985_11 |
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