HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- → HCID 20523549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- | HCID 89715 | — |
| Reactant | HCID 20523556 | HCID 20523556 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20523549 | HCID 20523549 | 59.7% |
Reaction Steps
A mixture of 2.91 g (0.01 mole) of 2-[(1-phenyl-2-pyrrolyl)carbonyl]benzoic acid prepared in part A above, 2.34 g (0.017 mole) of 84.6 percent active N,N,N',N'-tetramethyl-m-phenylenediamine in 4.0 ml of acetic anhydride was interacted in a manner similar to that described in Example 1, part C to obtain 2.61 g of 3-[2,4-bis(dimethylamino)phenyl]-3-(1-phenyl-2-pyrrolyl)phthalide (Formula IV: R0 =R1 =R2 =R3 =H; R=CH3 ; R4 =N(CH3)2 ; R7 =C6H5), a peach-colored powder melting at 193°-194° C. The infrared spectrum showed a maximum at 1760 cm-1 (C=O; s). A toluene solution of this product spotted on silica gel developed an immediate orange-red-colored image.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04351768 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-cfcfe3ade44f48998778c1189525ad7d |
| Source note | uspto-grants-1982_09 |