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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941783Generated: November 2, 2026

Nitric Acid → 1-(2,3-Difluoro-5-nitrophenyl)ethanone

https://huagongshe.com/reaction/1941783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178466552HCID 178466552—
SolventSulfuric AcidHCID 1118—
Product1-(2,3-Difluoro-5-nitrophenyl)ethanoneHCID 5747586528%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under an inert atmosphere of nitrogen 1-(2,3-difluoro-phenyl)-ethanone (5.0 g (32 mmol) was added dropwise to sulphuric acid (95-97%, 20 ml), cooled to 0° C., at such a rate that the temperature was maintained below 5° C. Thereafter, the reaction mixture was cooled to −15° C. and a solution of nitric acid (3.22 ml, 46.4 mmol) in sulphuric acid (95-97%, 4.6 ml) was added dropwise at −15° C. After stirring at −10° C. for 45 minutes, the mixture was poured on ice. Ethyl acetate was added, then the organic layer separated, washed with water, dried over sodium sulphate, and evaporated at reduced pressure. Purification of the crude light yellow oil (5.64 g) by chromatography on silica gel using a gradient of heptane/ethyl acetate=100:0 to 0:100 yielded the 1-(2,3-difluoro-5-nitro-phenyl)-ethanone (1.83 g, 28% of theory) as a light yellow oil together with a mixture of 1-(2,3-difluoro-5-nitro-phenyl)-ethanone and 1-(2,3-difluoro-6-nitro-phenyl)-ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389513B2
Source datasetuspto-grants-2013_03
ORD IDord-82a723b392734ef39415a928ac534b32
Source noteuspto-grants-2013_03