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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750195Generated: October 28, 2026

Hydrochloric Acid → 4-[(1-Ethylpropyl)amino]-3-nitrobenzoic acid

https://huagongshe.com/reaction/1750195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86714408HCID 86714408—
SolventEthanolHCID 702—
Product4-[(1-Ethylpropyl)amino]-3-nitrobenzoic acidHCID 11514348100%

Reaction Steps

30.0 g of 4-(1-ethyl-propylamino)-3-nitro-benzoic acid ethyl ester were dissolved in 100 ml ethanol and 10 ml THF and 107 ml of 2 M aqueous sodium hydroxide solution were added. After stirring at room temperature over night, the reaction mixture was brought to pH 1 by addition of 2 M aqueous hydrochloric acid and extracted with ethyl acetate three times. The combined organic phases were dried over magnesium sulphate and concentrated to yield 27.0 g (100%) of 4-(1-ethyl-propylamino)-3-nitro-benzoic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156796B2
Source datasetuspto-grants-2015_10
ORD IDord-b6b6f9098bd14ff3acd106fe44f0f4bf
Source noteuspto-grants-2015_10