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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215119Generated: November 1, 2026

Hydrochloric Acid → 4-(2-Methoxyphenyl)-3-methylbenzoic acid

https://huagongshe.com/reaction/2215119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2'-methoxy-2-methylbiphenyl-4-carboxylateHCID 67528780—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methoxyphenyl)-3-methylbenzoic acidHCID 2194775989.2%

Reaction Steps

The (2-methyl-2′-methoxy-[1,1′-biphenyl]-4yl)carboxylic acid methyl ester of Step A (1.9 g, 7.4 mmol) was dissolved in tetrahydrofuran (30 mL) and 1 N sodium hydroxide (15 mL, 15 mmol) was added. The reaction mixture was heated at reflux overnight, then cooled and acidified with 2 N hydrochloric acid. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give 1.6 g of product as a white solid, m.p. 160–162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109193B2
Source datasetuspto-grants-2006_09
ORD IDord-8adb03a66f77466d9532c68860ee4f0a
Source noteuspto-grants-2006_09