HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889248Generated: October 31, 2026
Benzophenone imine → 3-Bromo-2-chloro-5-fluoroaniline
https://huagongshe.com/reaction/1889248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 1,3-Dibromo-2-chloro-5-fluorobenzene | HCID 2724604 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 86660290 | HCID 86660290 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Bromo-2-chloro-5-fluoroaniline | HCID 58553824 | — |
Reaction Steps
3-bromo-2-chloro-N-(diphenylmethylene)-5-fluoroaniline. A mixture of 2,6-dibromo-4-fluoro-1-chlorobenzene (865 mg, 3 mmol), benzophenone imine (0.61 ml, 3.6 mmol), Pd2(dba)3 (137 mg, 0.15 mmol), sodium t-butoxide (432 mg, 4.5 mmol), (S)-BINAP (280 mg, 0.45 mmol), and toluene (30 ml) was heated at 80° C. for 16 h. The mixture was extracted with ethyl acetate and the combined organic phase washed with brine. The organic phase was dried over sodium sulfate and concentrated. The crude product was purified by silica gel flash chromatography (40:1 to 20:1 hexanes/ethyl acetate eluant) to provide the title compound as a powder. MS m/z 388.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501758B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-1eb46b9cc7e34f7eb2962fa592896ad9 |
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| Source note | uspto-grants-2013_08 |
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