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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384814Generated: October 31, 2026

Hydrochloric Acid → 4-(2-Chloroethoxy)-3-methoxybenzoic acid

https://huagongshe.com/reaction/384814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-Chloro-ethoxy)-5-methoxy-benzoic acid methyl esterHCID 23033016—
SolventMethanolHCID 887—
Product4-(2-Chloroethoxy)-3-methoxybenzoic acidHCID 2246667196.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

In a 300 mL volume glass flask equipped with a stirrer, a thermometer and a dropping funnel were placed 17.40 g (69.7 mmol) of methyl 4-(2-chloroethoxy)-3-methoxybenzoate, 69.7 mL of aqueous sodium hydroxide solution (2 mol/L), and 69.7 mL of methanol. The resulting mixture was heated to 40° C. for 4 hours in an argon gas atmosphere. After the reaction was complete, the reaction mixture was cooled to 10° C., and neutralized by 69.7 mL of hydrochloric acid (2 mol/L). The reaction mixture was then placed to distill methanol off, and cooled to 10° C., to precipitate a crystalline product. The crystalline product was collected and dried under reduced pressure, to give 15.5 g (isolated yield: 95.2%, purity: 99% in terms of area percentage by high performance liquid chromatography) of 4-(2-chloroethoxy)-3-methoxybenzoic acid as a white crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367824B2
Source datasetuspto-grants-2013_02
ORD IDord-11e2d3978e81461bbf9af2c5c984e595
Source noteuspto-grants-2013_02