HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368799Generated: October 30, 2026
2-Methyl-3-nitrobenzoic acid → 3-Hydroxy-2-methylbenzoic Acid
https://huagongshe.com/reaction/368799
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-3-nitrobenzoic acid | HCID 16096 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 3-Hydroxy-2-methylbenzoic Acid | HCID 252023 | — |
Reaction Steps
3-Nitro-2-methyl benzoic acid (90.5 g, 0.500 mol) was dissolved in 1.0 mol/L aqueous solution (500 ml) of sodium hydroxide. 10% Palladium-carbon (4.5 g) was added and the mixture was stirred under a hydrogen atmosphere (2-3 atm) for 9 hours at 40° C. The catalyst was filtered off and conc. sulfuric acid (94.0 ml) was added under ice-cooling. An aqueous solution of sodium nitrite (35.0 g, 0.500 mol/150 ml) was added over one hour while stirring the mixture at riot more than 6° C., and after the dropwise addition, the mixture was heated at 65° C. for 1.5 hours. The inner temperature rose to 57° C. in an hour. The reaction mixture was cooled to room temperature, and saturated brine (300 ml) was added. The mixture was extracted with ethyl acetate (700 ml). The organic layer was washed with saturated brine (200 ml) and dried over magnesium sulfate. The solvent was distilled away to give 3-hydroxy-2-methyl benzoic acid as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133461 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-151c97eb709142f3b5da62beabef8d0c |
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| Source note | uspto-grants-2000_10 |
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