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
Firstly 25.6 g (0.25 mol) of acetic anhydride and then 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 initially introduced concentrated sulphuric acid. After the reaction mixture had been further stirred for 4 hours, 150 g of ice-water were added to it and it was thoroughly stirred. The precipitated reaction product was filtered off under suction, washed with 100 ml of water and dried. 37.0 g (86.5% of theory) of trimethylpyruvic acid N-acetylamide were obtained as colorless shiny platelets of melting point 82° to 84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04408044 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-9e02003dfc9a44e48206f8ccd084de93 |
| Source note | uspto-grants-1983_10 |