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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66248생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/66248

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물Ammonium BromideHCID 25514—
반응물2,4,6-Triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidineHCID 20527890—
용매MethanolHCID 887—
생성물2,6-Diethyl-2,3,6-trimethylpiperidin-4-oneHCID 22182213—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04131599
출처 데이터셋uspto-grants-1978_12
ORD IDord-df2a8612cfb84b0fbe5a33693f26d1b4
출처 메모uspto-grants-1978_12