Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Dimethylaminoacrylonitrile | HCID 5324735 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86748203 | HCID 86748203 | 97.2% |
Reaction Steps
A solution of oxalyl chloride (13.1 mL, 0.15 mol) in 1,2-dichloroethane is added dropwise to a solution of N,N-dimethylformamide (11.6 mL, 0.15 mol) in 1,2-dichloroethane while maintaining the reaction mixture temperature below 0° C. The reaction mixture is stirred for 45 minutes, treated with a solution of trans-3-dimethylaminoacrylonitrile (16.4 mL, 0.15 mol) in 1,2-dichloroethane, stirred at room temperature for 16 hours, refluxed for two hours and concentrated in vacuo to obtain a semi-solid residue. A solution of the residue in 2-propanol is treated with a solution of oxalic acid dihydrate (18.9 g, 0.15 mol) in 2-propanol and warmed until a clear solution is obtained. The clear solution is cooled to and held at room temperature for several hours, cooled in a freezer for two hours and filtered. The filter cake is washed sequentially with 2-propanol and ether and dried in a vacuum desiccator at 50° to give the title product (28.6 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05359089 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-bf78782cf64f4be3bbe81445ac34a6ae |
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| Source note | uspto-grants-1994_10 |
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