HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dichlorophenol → 1,2,4-Trichlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dichlorophenol | HCID 66 | — |
| Reactant | 2,4-Dichlorophenol | HCID 8449 | — |
| Reactant | 4-Bromo-2,5-dichlorophenol | HCID 16022 | — |
| Product | 1,2,4-Trichlorobenzene | HCID 13 | — |
Reaction Steps
A process for the preparation of 4-bromo-2,5-dichlorophenol which comprises reacting a mixture of 2,5-dichlorophenol and 2,4-dichlorophenol obtained by saponifying 1,2,4-trichlorobenzene and distilling 3,4-dichlorophenol from the resulting mixture, with an equimolar amount of bromine in a glacial acetic acid reaction medium at a temperature of about 30° C. and thereafter recovering the 4-bromo-2,5-dichlorophenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04067913 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-2a685b9601db4566bc56613816c67c42 |
| Source note | uspto-grants-1978_01 |