HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 178477296, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 178485491 | HCID 178485491 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178477296 | HCID 178477296 | — |
Reaction Steps
5.02 g (20 mmols) of 3,5-dinitrophthalic acid N-methylimide, 2.73 g (44 mmols) of ethylmercaptan, 8.2 g (1 0 mmols) of anhydrous sodium acetate and 50 ml of ethyl acetate are kept at 25° C. overnight and then kept under reflux, again overnight. The reaction mixture is evaporated, the residue is taken up in methylene chloride/water, the extracts are washed with saturated NaHCO3 solution, dried over sodium sulfate and evaporated and the residue is chromatographed with methylene chloride over 20 g of silica gel. After recrystallisation from methylene chloride/n-pentane, 2.40 g (45% of theory) of 3-ethylthio-5-nitrophthalic acid N-methylimide, with a melting point of 193°-4° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04480105 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-55661acaf59b4bdd914b876877a43d07 |
| Source note | uspto-grants-1984_10 |