HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22076399, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22918353 | HCID 22918353 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22076399 | HCID 22076399 | — |
Reaction Steps
A steady stream of argon is passed through a suspension of 23.4 g (67.18 mmol) of 4,5-bis(anilino)phthalic acid in 250 ml of toluene, and 19.0 ml (201.5 mmol, 3 eq) of acetic anhydride is added. The reaction mixture is heated to 60°-65° for 90 minutes with vigorous stirring. Thereaction mixture is cooled to 10° for 30 minutes, and the yellow to orange crystals are filtered off and washed with toluene/hexane to yield the title compound in the form of yellow crystals, FAB-MS: 331 [M+ +H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05491144 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-1298ced3562b4a81b018cc3bcd18d542 |
| Source note | uspto-grants-1996_02 |