反应 #2122495

ord-e052a243bc8b449595334c5c76e1f5de

反应方程式

[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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

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

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08574607B2uspto-grants-2013_11