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Water → 8-Methyl-3,8-diazabicyclo(3.2.1)octane dihydrochloride

HRID 1605937
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인쇄 미리보기

반응식

HRID 1605937 반응식
O.[ClH:2].Cl.C([N:11]1[CH2:17][CH:16]2[N:18]([CH3:19])[CH:13]([CH2:14][CH2:15]2)[CH2:12]1)C1C=CC=CC=1.O>C(O)C.[Pd]>[ClH:2].[ClH:2].[CH3:19][N:18]1[CH:13]2[CH2:14][CH2:15][CH:16]1[CH2:17][NH:11][CH2:12]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 962WaterHCID 215454913-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride monohydrate

생성물 1

HCID 221201898-Methyl-3,8-diazabicyclo(3.2.1)octane dihydrochloride수율 152.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 3-benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride monohydrate (18.1 g, 0.059 mole) in absolute ethanol (200 ml) and 10% palladium on charcoal (3.0 g) was hydrogenated for 2 hours at atmospheric pressure. Sufficient water was added to dissolve the insoluble hydrochloride salt that had formed, and the reaction was filtered. The filtrate was evaporated in vacuo, the residue was triturated in hot absolute ethanol, and the mixture was filtered to yield 8.98 g of 8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride, melting point 315° C (dec.). The mother liquor was treated with ethanolic dry hydrogen chloride to afford an additional 2.28 g. Yield: 12.26 g (96%).

후처리

  1. customhad formed
  2. filtrationthe reaction was filtered
  3. customThe filtrate was evaporated in vacuo
  4. customthe residue was triturated in hot absolute ethanol
  5. filtrationthe mixture was filtered

출처 및 근거

ORD 기록
ord-f6e3cf663f174dc48486f036354f29ea
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03951980

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