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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528165Generated: November 4, 2026

Nitric Acid → 1-(2-Hydroxy-5-nitrophenyl)-2-methylpropan-1-one

https://huagongshe.com/reaction/1528165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactant1-(2-Hydroxyphenyl)-2-methyl-1-propanoneHCID 241555—
ReactantEthylacetate heptaneHCID 21899848—
SolventAcetic AcidHCID 176—
Product1-(2-Hydroxy-5-nitrophenyl)-2-methylpropan-1-oneHCID 13157008—
ProductHCID 89526327HCID 89526327—

Reaction Conditions

Temperature5 °C

Reaction Steps

1.6 ml of fuming nitric acid were added, over the course of 20 minutes, to a solution of 4.1 g of 1-(2-hydroxyphenyl)-2-methylpropan-1-one in 25 ml of acetic acid cooled to 5° C. The reaction medium was stirred at ambient temperature for 5 hours (followed by TLC, 10/1 heptane/ethyl acetate). The reaction was stopped before all the 1-(2-hydroxyphenyl)-2-methylpropan-1-one was consumed. The reaction medium was diluted with 70 ml of water and then extracted with ethyl acetate (4:1, 3×50 ml). The organic phases were combined, washed with water (20 ml) and then with a saturated sodium chloride solution (25 ml), and dried over magnesium sulfate. The solvent was evaporated off and the residue was chromatographed on silica. 1.40 g of 1-(2-hydroxy-5-nitrophenyl)-2-methylpropan-1-one and 1.2 g of 1-(2-hydroxy-3-nitrophenyl)-2-methylpropan-1-one were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090596B2
Source datasetuspto-grants-2015_07
ORD IDord-ac778bd2713a42988a1ceb72af474de8
Source noteuspto-grants-2015_07