HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 3-Chloro-5-iodoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | HCID 20472918 | HCID 20472918 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 3-Chloro-5-iodoaniline | HCID 15168449 | 90% |
Reaction Steps
55.5 parts of 4-bromo-3-chloro-5-iodoaniline, 250 parts of phenol, 8 parts of hydroiodic acid (57% strength) and 15 parts of ruthenium-on-charcoal catalyst (5% strength) are reacted with hydrogen under a pressure of 23 to 47 bars and at 145° C., during the course of 2 hours, whilst stirring. After the usual working up, 38 parts of 3-chloro-5-iodo-aniline are obtained. Yield: 90% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04429156 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-9cf97ab399b04d638639b3895dd121ba |
| Source note | uspto-grants-1984_01 |