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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-(4-hydroxy-3-nitrophenyl)acetateHCID 1473109—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-Hydroxy-3-nitrophenylacetic acidHCID 44736499.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544989B2
Source datasetuspto-grants-2003_04
ORD IDord-21d3cf9e814143948d12e097c1689b96
Source noteuspto-grants-2003_04