Formaldehyde → 2-[(4-Cyclohexylmethyl-1-piperidyl)methyl]propenenitrile

HRID 1390114Notes

Reaction equation

HRID 1390114 reaction equation
[C:1]([CH2:3][C:4](O)=O)#[N:2].O1CCOC[CH2:8]1.[CH:13]1([CH2:19][CH:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.C=O>O>[CH:13]1([CH2:19][CH:20]2[CH2:21][CH2:22][N:23]([CH2:8][C:3](=[CH2:4])[C:1]#[N:2])[CH2:24][CH2:25]2)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]1

Participants

6

Reactant 4

HCID 712FormaldehydeHCID 9740Cyanoacetic acidHCID 312751,4-DioxaneHCID 988834-(Cyclohexylmethyl)piperidine

Product 1

HCID 130410362-[(4-Cyclohexylmethyl-1-piperidyl)methyl]propenenitrile

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Cyanoacetic acid (0.9 g., 0.01 mole) was dissolved in 6 ml. of dioxane and 1 ml. of water. In a 15 minute period, 4-cyclohexylmethylpiperidine (1.8 g., 0.01 mole) was added. After an additional 15 minutes, 37% aqueous formaldehyde (1.8 g., 0.02 mole) was dripped in over a two minute period. The reaction mixture was agitated twelve hours at 20°-25° C., extracted with 200 ml. of ether, water washed, dried over anhydrous sodium sulfate, filtered and stripped. A yield of 1.2 g. of high purity product was obtained as a residue.

Workup

  1. customwas dripped in over a two minute period
  2. extractionextracted with 200 ml
  3. washof ether, water washed
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. customof high purity product was obtained as a residue

Sources & evidence

ORD record
ord-ec2e7d10b1cc4ec7a0faad16c483edc5
Source dataset
uspto-grants-1981_01
Patent number
US04247700

Reaction notes

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