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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154599Generated: October 30, 2026

Hydrochloric Acid → 4-(3-Formyl-4-nitro-phenoxy)-butyric acid

https://huagongshe.com/reaction/1154599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-((3-formyl-4-nitrophenyl)oxy)butyrateHCID 10588876—
SolventEthanolHCID 702—
Product4-(3-Formyl-4-nitro-phenoxy)-butyric acidHCID 275922794%

Reaction Steps

To a solution of ethyl 4-(3-formyl-4-nitrophenyl)oxybutyrate (65 g) in ethanol (400 ml) was added 3N NaOH (100 ml) in small portions. After 30 minutes at room temperature the reaction mixture was acidified with concentrated HCl and the ethanol evaporated. The aqueous residue was extracted with ethyl acetate (4×200 ml). The combined organic layers were washed with brine (2×200 ml), dried over Na2SO4, filtered and evaporated to give a light yellow solid. Trituration with ether afforded 4-(3-formyl-4-nitrophenyl)oxybutyric acid (55 g), m.p. 109°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490371
Source datasetuspto-grants-1984_12
ORD IDord-76da3dd575094b4e9dcdbce8b3a96605
Source noteuspto-grants-1984_12