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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant2-Bromo-4-(trifluoromethyl)benzoic acidHCID 67605—
Reactant2-Bromo-1-methyl-4-(trifluoromethyl)benzeneHCID 2779376—
ReactantTetraethylammonium permanganateHCID 11218887—
ReactantSodium BisulfiteHCID 23665763—
Product(2E)-3-[2-Bromo-4-(trifluoromethyl)phenyl]-N-indol-5-ylprop-2-enamideHCID 57807978—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582657B2
Source datasetuspto-grants-2009_09
ORD IDord-8ead1b3012a44d2ab1273c223c778832
Source noteuspto-grants-2009_09