HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,4,5-Tetrachlorobenzene → 2,4,5-Trichlorophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,4,5-Tetrachlorobenzene | HCID 7270 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 2,4,5-Trichlorophenol | HCID 7271 | — |
Reaction Steps
The presently employed technology to produce 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) and 2,4,5-trichlorophenol (2,4,5-TCP) commercially involves the dechlorination of 1,2,4,5-tetrachlorobenzene with aqueous sodium hydroxide or anhydrous sodium hydroxide in the presence of alcohols under elevated temperatures and pressures to form 2,4,5-TCP according to the reaction: ##STR2## Under the conditions of alkalinity, temperature and pressure, this process produces between 1 to 100 parts per million of the highly toxic teratogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) according to the reaction: ##STR3##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04345097 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-a5ea598de76f4ad5a088742a46523e79 |
| Source note | uspto-grants-1982_08 |