HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylamine → Acetic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | HCID 20534275 | HCID 20534275 | — |
| Reactant | HCID 20534282 | HCID 20534282 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20534283 | HCID 20534283 | — |
Reaction Steps
Following a procedure similar to that described in Example 3 but employing 1.6 g. of an isomer mixture comprising 3-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-4-pyridinecarboxylic acid and 4-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-3-pyridinecarboxylic acid, 0.9 g. of diphenylamine, 0.5 ml. of pyridine and 6 ml. of acetic anhydride there was obtained 1-(1-ethyl-2-methyl-3-indolyl)-1-(diphenylamino)furo[3,4-c]pyridine-3(1H)-one as a viscous oil. A toluene solution of the product contacted with acidic clay or phenolic resin developed an orange image.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243250 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-920756fe9b024854baa1d3512367edb7 |
| Source note | uspto-grants-1981_01 |