関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Ammonium Bromide | HCID 25514 | — |
| 反応物 | 2,4,6-Triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine | HCID 20527890 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2,6-Diethyl-2,3,6-trimethylpiperidin-4-one | HCID 22182213 | — |
反応手順
19.6 g of 2,4,6-triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine and 0.4 g of ammonium bromide were added to 200 ml of methanol. To the mixture was added dropwise 10 g of 37% hydrochloric acid at 10° C., with stirring. After completion of the addition the whole was stirred at room temperature for 4 hours and there was then added a further 20 ml of 18% hydrochloric acid. The mixture was then heated at 30°-40° C. for 7 hours and allowed to stand over night at room temperature. The mixture was made alkaline with 40% aqueous potassium carbonate solution and, after methanol has been distilled off under reduced pressure, the residue was extracted with ether. The ether solution was dried over potassium carbonate and the ether was removed. The residue was subjected to distillation under reduced pressure to yield 2,6-diethyl-2,3,6-trimethyl-4-oxopiperidine as an oil boiling at 91°-93° C./2 mm Hg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04131599 |
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| 出典データセット | uspto-grants-1978_12 |
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| ORD ID | ord-df2a8612cfb84b0fbe5a33693f26d1b4 |
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| 出典メモ | uspto-grants-1978_12 |
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