HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264621Generated: October 30, 2026
Hydrochloric Acid → 4-Hydroxy-3-nitrophenylacetic acid
https://huagongshe.com/reaction/1264621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-(4-hydroxy-3-nitrophenyl)acetate | HCID 1473109 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxy-3-nitrophenylacetic acid | HCID 447364 | 99.4% |
Reaction Steps
Methyl 4-hydroxy-3-nitrophenylacetate (21.1 g, 0.1 mol) was suspended in a mixture of water (55 ml) and methanol (105 ml). The suspension was stirred at room temperature while a solution of sodium hydroxide (8.8 g, 0.22 mol) in water (50 ml) was added dropwise over 20 minutes, maintaining the reaction temperature between 20 and 25° C. by water bath cooling. The resultant dark red solution was stirred at room temperature for 15 minutes, diluted with water and acidified to pH1-2 by addition of 2M hydrochloric acid and extracted with ethyl acetate. The organic extract was washed with brine (200 ml), dried over magnesium sulphate, filtered and concentrated under reduced pressure to give 4-hydroxy-3-nitrophenylacetic acid (19.6 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06544989B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-21d3cf9e814143948d12e097c1689b96 |
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| Source note | uspto-grants-2003_04 |
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