HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Phenyl-p-phenylenediamine → HCID 9814010, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Phenyl-p-phenylenediamine | HCID 7564 | — |
| Reactant | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| Reactant | HCID 131724457 | HCID 131724457 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 9814010 | HCID 9814010 | — |
Reaction Steps
A mixture of 1.84 g (10 mmoles) of N1-phenyl-1,4-benzenediamine and 0.41 ml (5 mmoles) of α-bromo-γ-butyrolactone in 20 ml of acetonitrile is heated under reflux for 5 hours. After returning to 20° C., the precipitate which appears during the reaction (N1-phenyl-1,4-benzenediamine hydrobromide) is filtered and rinsed with 20 ml of acetonitrile. The filtrate is concentrated to dryness under vacuum and the residue is purified on a silica column (eluent: Heptane/AcOEt: 1/1 to 4/6). Beige powder. Melting point: 142.5-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06747024B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-97014b1b27d74e67b887cb4af94907c1 |
| Source note | uspto-grants-2004_06 |