HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → N-tert-Butyl-3,3-dimethyl-2-oxobutanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 3,3-Dimethyl-2-oxobutanenitrile | HCID 94527 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-tert-Butyl-3,3-dimethyl-2-oxobutanamide | HCID 13355144 | — |
Reaction Steps
27.8 (0.25 mole) of pivaloyl cyanide, dissolved in 22 g (0.25 mole) of t-butyl methyl ether were added to a reaction mixture, which had been initially introduced into the reaction vessel, consisting of 37.5 g of concentrated sulphuric acid and 52.5 g of glacial acetic acid at 20° to 30° C. in the course of 30 minutes. After subsequently stirring the reaction mixture at room temperature for 2 hours, it was poured onto 125 g of ice and stirred thoroughly. The product which precipitated was filtered off, washed with water and dried. 40.8 g (87.5% of theory) of analytically pure trimethylpyruvic acid N-tert.-butylamide with a melting point of 65° C. and a content of >99% (determined by gas chromatography) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04345100 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-89f5f9d49d7f41f38de44e6c05b4f2eb |
| Source note | uspto-grants-1982_08 |