HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3,3-Bis(2,4-bis(dimethylamino)phenyl)-5-(dimethylamino)phthalide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- | HCID 89715 | — |
| Reactant | HCID 23343387 | HCID 23343387 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3,3-Bis(2,4-bis(dimethylamino)phenyl)-5-(dimethylamino)phthalide | HCID 54137693 | — |
Reaction Steps
A mixture of 2-(2,4-bis(dimethylamino)benzoyl)-4-(dimethylamino)benzoic acid or the 5-(dimethylamino) isomer thereof (10 g.), N,N,N'-tetramethyl-m-phenylenediamine (2.30 g.) and acetic anhydride (50 ml.) was warmed (at 30°-35° C.) during one hour. More N,N,N',N'-tetramethyl-m-phenylenediamine (1.15 g.) was added and warming was continued. The mixture was diluted with dilute hydrochloric acid (10%) and ice and filtered. The filtrate was made alkaline. Crystallization of the product from toluene afforded 3,3-bis(2,4-bis(dimethylamino)phenyl)-5-(dimethylamino)phthalide (I: X=Y2 =Y4 =Z5 =(CH3)2N, Z4 =Z6 =Z7 =H) (m.p. 188°-192° C.) or the 6-(dimethylamino) isomer thereof.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220357 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-ed9ba44a51ff4e5499a2386ec0550278 |
| Source note | uspto-grants-1980_09 |