HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylamine → Acetic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | HCID 20534284 | HCID 20534284 | — |
| Reactant | HCID 20534307 | HCID 20534307 | — |
| Product | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20534291 | HCID 20534291 | — |
| Product | HCID 20534333 | HCID 20534333 | — |
Reaction Steps
Following a procedure similar to that described in Example 3 but employing 1.6 g. of an isomer mixture comprising 3-[4-(diethylamino)-2-methylbenzoyl]-4-pyridinecarboxylic acid and 4-[4-(diethylamino)-2-methylbenzoyl]-3-pyridinecarboxylic acid, 0.9 g. of diphenylamine and 6 ml. of acetic anhydride there was obtained an isomer mixture comprising 3-[4-(diethylamino)-2-methylphenyl]-3-(diphenylamino)furo[3,4-c]pyridine-1(3H)-one and 1-[4-(diethylamino)-2-methylphenyl]-1-(diphenylamino)furo[3,4-c]pyridine-3(1H)-one. A toluene solution of the product contacted with acidic clay or phenolic resin developed a red-grape image.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243250 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-cfa80065610f44eca3b1b32913bbadc0 |
| Source note | uspto-grants-1981_01 |