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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 1-(2-Hydroxyphenyl)-2-methyl-1-propanone | HCID 241555 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(2-Hydroxy-5-nitrophenyl)-2-methylpropan-1-one | HCID 13157008 | — |
| Product | HCID 89526327 | HCID 89526327 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090596B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-ac778bd2713a42988a1ceb72af474de8 |
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| Source note | uspto-grants-2015_07 |
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