Reaction equation
[C:1]([CH2:3][C:4](O)=O)#[N:2].[NH:7]1[CH2:15][CH2:14][CH:10]([C:11]([OH:13])=[O:12])[CH2:9][CH2:8]1.[CH2:16]=O.[Cl-].[Na+]>C(Cl)Cl.O1CCOCC1>[C:11]([CH:10]1[CH2:14][CH2:15][N:7]([CH2:16][C:3](=[CH2:4])[C:1]#[N:2])[CH2:8][CH2:9]1)([OH:13])=[O:12]Participants
7
Conditions
- Temperature
- 35 °C
Procedure
Cyanoacetic acid (12.8 g. 0.15 mole) was dissolved in 25 ml. of dioxane. Next, isonipecotic acid (19.4 g., 0.15 mole) was added. Then, 37% aqueous formaldehyde (25 g., 0.3 mole) was dripped in and the temperature maintained at a maximum of 35° C. After mixing overnight sodium chloride was added to saturation and methylene chloride used to extract the mixture. The organic phase was washed with water, dried over anhydrous sodium sulfate and after filtration, concentrated. Most of the product appeared in the aqueous phase. This was extracted twice with 500 ml. of methylene chloride in a continuous extractor. The residue obtained after solvent removal weighed 14.2 g., m.p. 109°-111° C. of analytical purity.
Workup
- extractionto extract the mixture
- washThe organic phase was washed with water
- dry with materialdried over anhydrous sodium sulfate
- filtrationafter filtration
- concentrationconcentrated
- extractionThis was extracted twice with 500 ml
- customThe residue obtained
- customafter solvent removal
Sources & evidence
- ORD record
- ord-6bd5bd60a0f443a8943465267abf582a
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04342872
Linked notes
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