반응 #2122495

ord-e052a243bc8b449595334c5c76e1f5de

반응 방정식

[C-]#N.[K+]
potassium cyanide
O=S([O-])O.[Na+]
sodium bisulfite
CCON1CCC(=O)CC1
1-ethoxy-piperidin-4-one
CCON1CCC(O)(C#N)CC1
1-Ethoxy-4-hydroxy-piperidine-4-carbonitrile

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.WAITleft
  3. 3
    workup.STIRRINGstirring for 24 hours
  4. 4
    추출The mixture was thoroughly extracted with ethyl acetate (4×30 ml)
  5. 5
    세척the combined organic layers were washed twice with brine (2×30 ml)
  6. 6
    건조dried over sodium sulfate
  7. 7
    여과After filtration and concentration under vacuum
  8. 8
    기타the residue was purified by column chromatography on silica gel

실험 절차

A solution of sodium bisulfite (10.7 g, 103 mmol) in 10 ml of water was cooled in an ice bath. Then, 1-ethoxy-piperidin-4-one (12.3 g, 86 mmol, prepared according to J. Org. Chem. 1961, 26, 1867-74) was added dropwise. After the addition, the mixture was stirred for another 30 min. A solution of potassium cyanide (8.4 g, 129 mmol) in 10 ml of water was added slowly, the reaction mixture was warmed up to room temperature and left stirring for 24 hours. The mixture was thoroughly extracted with ethyl acetate (4×30 ml) and the combined organic layers were washed twice with brine (2×30 ml) and dried over sodium sulfate. After filtration and concentration under vacuum, the residue was purified by column chromatography on silica gel. Yield: 13.2 g of 1-ethoxy-4-hydroxy-piperidine-4-carbonitrile (title compound P4.9) as a light yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08574607B2uspto-grants-2013_11