HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → trimethylpyruvic acid N-acetylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3,3-Dimethyl-2-oxobutanenitrile | HCID 94527 | — |
| Product | trimethylpyruvic acid N-acetylamide | HCID 12769196 | 86.5% |
Reaction Steps
First 25.6 g (0.25 mole) of acetic anhydride and then 27.8 g (0.25 mole) of pivaloyl cyanide were introduced, in each case at room temperature, into 49.0 g (0.5 mole) of concentrated sulphuric acid already in the reaction vessel. After subsequently stirring the reaction mixture for 4 hours, 150 g of ice-water were added and the mixture was stirred thoroughly. The reaction product which precipitated was filtered off, washed with 100 ml of water and dried. 37.0 g (86.5% of theory) of trimethylpyruvic acid N-acetylamide were obtained as colorless, glistening flakes of melting point 82° to 84° C.; content according to determination by gas chromatography: >99%. No additional purification operations were required for further reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370498 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-76f9b6f71dcf44bd8842fd8c2311c00f |
| Source note | uspto-grants-1983_01 |