HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22076403, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22918423 | HCID 22918423 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22076403 | HCID 22076403 | — |
Reaction Steps
A steady stream of argon is passed through a suspension of 4.49 g (11.68 mmol) of 4,5-bis(4-fluoroanilino)phthalic acid in 75 ml of toluene and 3.32 ml (35.12 mmol, 3 eq) of acetic anhydride is added. The reaction mixture is heated to 60°-65° for 90 minutes with vigorous stirring. The reaction mixture is cooled to 10° for 15 minutes, theyellow orange crystals are filtered off and washed with toluene/hexane to yield the title compound in the form of yellow orange crystals, FAB-MS: 367 [M+ +H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05491144 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-bff1a6ae37584958b651d940696671e6 |
| Source note | uspto-grants-1996_02 |