HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718809Generated: October 23, 2026
Nitric Acid → 4-(4-Methyl-3-nitrophenyl)-4-oxobutanoic acid
https://huagongshe.com/en/reaction/718809
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 4-(4-Methylphenyl)-4-oxobutanoic acid | HCID 244162 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 4-(4-Methyl-3-nitrophenyl)-4-oxobutanoic acid | HCID 82116828 | 69% |
Reaction Steps
HNO3 (65%) (2300 mL) was cooled to about 0° C. Fuming HNO3 (5700 mL) was carefully added maintaining an internal temperature of less than 15° C. The solution was cooled to about −5° C. and H2SO4 (800 mL) was added maintaining an internal temperature of less than 5° C. After cooling to about −8° C., 4-oxo-4-(p-tolyl)butanoic acid (72) (4000 g, 20.8 mol) was added portionwise maintaining the temperature below about 0° C. After completion of addition the mixture was allowed to warm to about 15-17° C. The solution was poured onto crushed ice with stirring. After about 2 h at rt, the solid was collected by filtration washing with water (3×10 L) and then dried to afford 4-(4-methyl-3-nitrophenyl)-4-oxobutanoic acid (73) (3400 g, 69% yield). 1H NMR (300 MHz, DMSO): δ 8.46 (s, 1H), 8.20 (d, J=8.4 Hz, 1H), 7.64 (d, J=8.0 Hz, 1H), 3.25 (m, 2H), 2.62 (m, 2H), 2.60 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193744B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-dc191878323f4981b331d38ebff37f3c |
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| Source note | uspto-grants-2015_11 |
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