HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700859Generated: October 31, 2026
1,3-Dibromo-5,5-dimethylhydantoin → 1-Bromo-3,5-bis(trifluoromethyl)benzene
https://huagongshe.com/reaction/1700859
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | Benzene, 1,3-bis(trifluoromethyl)- | HCID 223106 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Bromo-3,5-bis(trifluoromethyl)benzene | HCID 67602 | — |
Reaction Steps
To glacial acetic acid (22.0 mL), cooled to 15° C. in a 1 L 3-n RB flask (equipped with mechanical stirrer, thermocouple, and addition funnel), was added concentrated (96%) sulfuric acid (142 mL) in one portion. An exothermic heat of solution raised the temperature to 35° C. After cooling to 25° C., 1,3-bis(trifluoro-methyl)benzene (107 g, 500 mmol) was added. With the acid mixture rapidly stirring, 1,3-dibromo-5,5-dimethylhydantoin (77.25 g; 270 mmol) was added over 2 min to give a multiple phase mixture (solid and two liquid). An exothermic reaction occured that raised the internal temperature to ˜40° C. (jacket cooling at 15° C.). After the reaction temperature began to drop (after 5 min) the reaction mixture was maintained at 45° C. for 4.5 hr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350915B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-7322aabdf3f94ec4bd47e3666bbe791f |
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| Source note | uspto-grants-2002_02 |
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