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
25.6 g (0.25 mol) of acetic anhydride, followed by 27.8 g (0.25 mol) of pivaloyl cyanide, were introduced, in each case at room temperature, into 49.0 g (0.5 mol) of concentrated sulphuric acid. After a further 4 hours' stirring, 150 g of ice water were added to the reaction mixture and the batch was stirred thoroughly. The reaction product which precipitated was filtered off, washed with 100 ml of water and dried. 37.0 g (86% of theory) of trimethylpyruvic acid N-acetylamide were obtained as colorless glistening flakes of melting point 82° to 84° C.; purity, according to gas-chromatographic determination,>98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980479 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-7f1a5593bdc04162a81f32b3fdaa789e |
| Source note | uspto-grants-1990_12 |