HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → N-(4-iodophenyl)1,2-diaminobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | N-(4-iodophenyl)-2-nitroaniline | HCID 15045509 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-iodophenyl)1,2-diaminobenzene | HCID 15045510 | — |
Reaction Steps
According to the method of Chem. Abs., 1962, 57, 9840a, a solution of sodium dithionite (85%, 24.74 g, 121 mmol) in water (120 ml) was added to a suspension of (4-iodophenyl)-2-nitroaniline in ethanol (500 ml). The mixture was heated under reflux for 45 minutes, cooled, treated with 300 ml of dilute aqueous ammonia, and concentrated under reduced pressure. The resulting white slurry was treated with 200 ml of dilute aqueous ammonia, filtered and washed with water (200 ml). The solid was dried in a vacuum desiccator at room temperature to give N-(4-iodophenyl)1,2-diaminobenzene, 8.91 g, which gradually darkens on exposure to light, m.p. 122°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05063237 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-b6272c44ad9244e99d351a2e29e8fe17 |
| Source note | uspto-grants-1991_11 |