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HRID 66248作成日:2026年10月26日

Hydrochloric Acid → 2,6-Diethyl-2,3,6-trimethylpiperidin-4-one

https://huagongshe.com/reaction/66248

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物Ammonium BromideHCID 25514—
反応物2,4,6-Triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidineHCID 20527890—
溶媒MethanolHCID 887—
生成物2,6-Diethyl-2,3,6-trimethylpiperidin-4-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04131599
出典データセットuspto-grants-1978_12
ORD IDord-df2a8612cfb84b0fbe5a33693f26d1b4
出典メモuspto-grants-1978_12