HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380225Generated: October 31, 2026
Bromide ion → 2-(Trifluoromethyl)benzoyl chloride
https://huagongshe.com/reaction/1380225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | 2-(Trifluoromethyl)benzoyl fluoride | HCID 67563 | — |
| Reactant | 2-(Trichloromethyl)benzoyl chloride | HCID 3016752 | — |
| Reactant | HCID 23326120 | HCID 23326120 | — |
| Product | 2-(Trifluoromethyl)benzoyl chloride | HCID 67561 | 400% |
Reaction Steps
Under ideal stoichiometic conditions three moles of trifluoromethylbenzoyl fluoride are contacted with one mole of trichloromethylbenzoyl chloride or tribromomethylbenzoyl bromide in the presence of a halogen transfer catalyst to yield four moles of trifluoromethylbenzoyl chloride or bromide. It will be understood however, that greater or less than stoichiometric amounts of the reactants can be employed. Thus, in accordance with the process of this invention substituted or unsubstituted trichloromethylbenzoyl chloride or tribromomethylbenzoyl bromide may be reacted with corresponding substituted or unsubstituted trifluoromethylbenzoyl fluorides, in the presence of a halogen transfer catalyst to produce the corresponding substituted or unsubstituted trifluoromethylbenzoyl chloride or bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04581179 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-70ee7774522b4711805fb2b1963f4bfa |
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| Source note | uspto-grants-1986_04 |
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