Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Mercaptoacetaldehyde | HCID 77775 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | HCID 1477332 | HCID 1477332 | — |
Reaction Steps
The 2-amino-3:5-dinitrothiophene used in the above Example was obtained by reacting the sodium salt of cyanoacetic acid with the dimer of mercaptoacetaldehyde in aqueous medium at 80° C., cooling to 20° C., adding acetic anhydride whilst maintaining the pH of the mixture between 6 and 7, acidifying and isolating the 2-acetylaminothiophene-3-carboxylic acid. This was then dinitrated in sulphuric acid medium at 0° C., the resulting 2-acetylamino-3:5-dinitrothiophene isolated and then deacylated by heating in an aqueous solution of sulphuric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04211696 |
|---|
| Source dataset | uspto-grants-1980_07 |
|---|
| ORD ID | ord-623dc4af1bdf40108f55745b0d03ce9c |
|---|
| Source note | uspto-grants-1980_07 |
|---|