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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958683Generated: October 31, 2026

4-Methoxyphenylacetic Acid → HCID 67184281, compound

https://huagongshe.com/reaction/1958683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxyphenylacetic AcidHCID 7690—
ReactantMethyl 2-chlorobenzoateHCID 11895—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 6930993HCID 6930993—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67184281HCID 67184281—

Reaction Conditions

Temperature55 °C

Reaction Steps

5-(2-Chlorophenyl)-4-(4-methoxyphenyl)thiophene-2-carboxylic acid is prepared, according to the procedure used in stages 1A)-1E), from (4-methoxyphenyl)acetic acid and methyl 2-chlorobenzoate. In the final stage of this procedure, 5 g of methyl 542-chlorophenyl)-4-(4-methoxyphenyl)-2-thiophenecarboxylate and 1.11 g of sodium hydroxide pellets are added to 30 ml of methanol and 3 ml of dioxane. The reaction medium is heated at 50-60° C. for 5 hours. It is evaporated to dryness, water is added and the impurities are extracted with ether. The aqueous phase is acidified and the expected compound is extracted with ether. After drying and evaporating, 3.5 g of the expected compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410137B2
Source datasetuspto-grants-2013_04
ORD IDord-0181be645ad54182b57b81c5e8d0686a
Source noteuspto-grants-2013_04