HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186441Generated: October 30, 2026
Acetic Acid → 1-Bromo-3,5-bis(trifluoromethyl)benzene
https://huagongshe.com/reaction/2186441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | Benzene, 1,3-bis(trifluoromethyl)- | HCID 223106 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromo-3,5-bis(trifluoromethyl)benzene | HCID 67602 | 94% |
Reaction Steps
A vigorously stirred solution of 1,3-bis(trifluoromethyl)benzene (107 g) in a mixture of glacial acetic acid (22 mL) and concentrated sulfuric acid (142 mL) was added 1,3-dibromo-5,5-dimethylhydantoin (77.25g) at 25° C. The exothermic reaction raised the temperature to approximately 40° C. After aging at 45° C. for 4.5 h, the mixture was cooled to approximately 0° C. and poured into cold water (250 mL). After washing with 5N NaOH (75 mL) the organic layer contained 137 g of the desired 3,5-bis(trifluoromethyl)-1-bromobenzene by assay (94% yield). This product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403793B2 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-48dd42a30cf0419b880d428e5391d68d |
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| Source note | uspto-grants-2002_06 |
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