HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090540Generated: November 1, 2026
1-Bromo-3,5-bis(trifluoromethyl)benzene → 3',5'-Bis(trifluoromethyl)-2-aminobenzophenone
https://huagongshe.com/reaction/2090540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3,5-bis(trifluoromethyl)benzene | HCID 67602 | — |
| Reactant | 2-amino-N-methoxy-N-methylbenzamide | HCID 11052242 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3',5'-Bis(trifluoromethyl)-2-aminobenzophenone | HCID 86651363 | 97.1% |
Reaction Steps
Then, in a nitrogen atmosphere, N-methoxy-N-methyl-anthranilamide (0.62 g, 3.4 mmol), and 3,5-bis(trifluoromethyl)-1-bromobenzene (1.00 g, 3.4 mmol) were dissolved in tetrahydrofuran (20 mL), followed by stirring at −78° C. To the solution, 1.66 mol/L n-butyl lithium (4.11 mL, 6.8 mmol) was gradually added dropwise, followed by stirring for 30 minutes. The reaction was terminated by adding 1 mol/L hydrochloric acid. The reaction solution was extracted with ethyl acetate. The organic layer was washed with a sodium chloride solution and then dried with magnesium sulfate, followed by filtration. The filtrate was concentrated using a rotary evaporator. The residue was purified by recrystallization (hexane). Thus, 3′,5′-bis(trifluoromethyl)-2-aminobenzophenone (1.1 g, 3.3 mmol) was obtained in a yield of 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436173B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-50704c5c022843f89b42e68fd22c924e |
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| Source note | uspto-grants-2013_05 |
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