HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Butanamide, N,N-diethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-ButenaMide, N,N-diethyl-, (E)- | HCID 5354453 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Butanamide, N,N-diethyl- | HCID 66192 | — |
| Product | N,N-Diethylbut-3-enamide | HCID 12545744 | — |
Reaction Steps
56.5 g of crotonic acid diethylamide 36.9 g of ethanol, 1.27 g of pyridine and 2.74 g of Co2 (CO)8 are reacted analogously to Example 1 for 1.5 hours at 170° C. under a carbon monoxide pressure of 150 bar (+approx. 2% by volume of hydrogen). Analysis showed that 99.6 mol % of the crotonic acid diethylamide had reacted. Relative to this, C5 -dicarboxylic acid derivatives containing mixed derivative groups had been formed at a selectivity of conversion of 97.4 mol %; 2-methylsuccinic acid 1-ethylester-4-diethylamide was 93.6% of this. In addition, butyric acid diethylamide and but-3-enoic acid diethylamide had been formed at selectivities of conversion of 1.2 mol % and 0.4 mol %, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588833 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-d8a8898b7e9a43319fd2142c67bb9229 |
| Source note | uspto-grants-1986_05 |