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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098321Generated: October 25, 2026

Hydrochloric Acid → HCID 10353361, compound

https://huagongshe.com/reaction/1098321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitromethaneHCID 6375—
ReactantSodium hydrideHCID 24758—
ReactantPhenyl 2,4,5-trifluorobenzoateHCID 10354819—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductHCID 10353361HCID 10353361—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (12 g, 60% in oil, 297 mmol) was rinsed with hexane (4×100 mL), flushed with anhydrous nitrogen, suspended in N,N-dimethylformamide (350 mL) and then treated with nitromethane (44 mL, 81 mmol). The resultant mixture was stirred at room temperature for 2.5 hours, cooled to 0° C. and then treated with a solution of phenyl 2,4,5-trifluorobenzoate (22.8 g, 90.0 mmol) in N,N-dimethylformamide (180 mL) over a period of two hours. The reaction mixture was kept at the same temperature overnight and stirring continued for an additional hour at room temperature. The mixture was poured into ice (400 g) with conc. hydrochloric acid (48 mL). The aqueous mixture was extracted with ethyl acetate (3×250 mL). The combined organic layers were washed with brine (40 mL), dried over anhydrous sodium sulfate, filtered, and evaporated under reduced pressure. The crude product was dissolved in ether-hexane (1:1, 240 mL) and water (200 mL). The organic layer was separated, and the crystals which formed upon standing and cooling in the freezer were recovered by filtration and dried to yield 2-nitro-1-(2,4,5-trifluorophenyl)ethanone as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143289B2
Source datasetuspto-grants-2012_03
ORD IDord-84bf9c4a748c441f946689ec9655e2f2
Source noteuspto-grants-2012_03