HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730288Generated: October 26, 2026
Hydrochloric Acid → (2E)-3-[2-Bromo-4-(trifluoromethyl)phenyl]-N-indol-5-ylprop-2-enamide
https://huagongshe.com/reaction/730288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Bromo-4-(trifluoromethyl)benzoic acid | HCID 67605 | — |
| Reactant | 2-Bromo-1-methyl-4-(trifluoromethyl)benzene | HCID 2779376 | — |
| Reactant | Tetraethylammonium permanganate | HCID 11218887 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Product | (2E)-3-[2-Bromo-4-(trifluoromethyl)phenyl]-N-indol-5-ylprop-2-enamide | HCID 57807978 | — |
Reaction Steps
2-Bromo-4-(trifluoromethyl)benzoic acid. To a solution of 2-bromo-1-methyl-4-trifluoromethylbenzene (7.6 g, 32 mmol, ABCR) in pyridine (75 mL) was added tetraethylammonium permanganate (24 g, 96 mmol, prepared according to the procedure of Sala, et al. J. Chem. Soc., Chem. Comm. 1978, 253). The reaction mixture was warmed to 70° C. and stirred at that temperature for 30 h. The reaction mixture was allowed to cool to 25° C. and poured into an ice bath containing cond HCl (150 mL) and NaHSO3 (150 g). The mixture turned to a clear aqueous solution and was extracted with EtOAc (4×200 mL). The combined extracts were washed with satd NaCl (200 mL), dried over Na2SO4, filtered and concentrated in vacuo to provide the title product as a white solid. MS (ESI, neg. ion) m/z: 267 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582657B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-8ead1b3012a44d2ab1273c223c778832 |
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| Source note | uspto-grants-2009_09 |
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