반응 #657281

ord-2765255ef40248b6960128160bcaf623

반응 방정식

CON1CCC(=O)CC1
1-methoxy-piperidin-4-one
CN
methylamine
CN.Cl
methylamine hydrochloride
[C-]#N.[K+]
potassium cyanide
CN.Cl
methylamine hydrochloride
CN
methylamine
[C-]#N.[K+]
potassium cyanide
CNC1(C#N)CCN(OC)CC1
1-methoxy-4-methylamino-piperidine-4-carbonitrile

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirring
  2. 2
    기타continued at room temperature until the reaction
  3. 3
    추출The aqueous reaction mixture was extracted with dichloromethane (1×500 ml, and 4×200 ml)
  4. 4
    건조the combined organic phases dried over sodium sulfate
  5. 5
    기타evaporated
  6. 6
    기타This material was used without further purification in the next step

실험 절차

To a solution of 1-methoxy-piperidin-4-one [prepared according to Journal of Organic Chemistry (1961), 26, 1867-74] (100 g, 0.77 mol), aqueous methylamine (40 wt. % in H2O, 86 ml) and methylamine hydrochloride (57.5 g, 0.85 mol) in water (700 ml) at 0° C. was added a solution of potassium cyanide (55.5 g, 0.85 mol) in water (150 ml) dropwise over one hour. The reaction mixture was stirred at room temperature for two days. Over the next five days, the mixture was further treated with methylamine hydrochloride (5×2.6 g, total 13.0 g), aqueous methylamine (5×4.3 ml, total 21.5 ml) and potassium cyanide (5×2.5 g, total 12.5 g), and stirring continued at room temperature until the reaction was judged complete by thin layer chromatography. The aqueous reaction mixture was extracted with dichloromethane (1×500 ml, and 4×200 ml), the combined organic phases dried over sodium sulfate and evaporated. Yield: 113.0 g of 1-methoxy-4-methylamino-piperidine-4-carbonitrile (compound P5.1) as a red liquid. This material was used without further purification in the next step.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09023760B2uspto-grants-2015_05