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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377677Generated: October 31, 2026

Hydrochloric Acid → 3-Methoxy-4-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/1377677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantDimethyl 2-methoxybenzene-1,4-dicarboxylateHCID 18677354—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxy-4-(methoxycarbonyl)benzoic acidHCID 12398305—

Reaction Steps

2-Methoxy-1,4-bis (methoxycarbonyl)benzene (1.61 g, 7.20 mmol) from Step 2 was dissolved in 20 mL of 1:1 THF:H2O and to the stirred solution was added 1N NaOH (7.2 mL, 7.2 mmol). After 24 h, the reaction was acidified to pH 2 with 1N HCl. The reaction was concentrated under reduced pressure and then extracted with CHCl3. The CHCl3 layer was dried (MgSO4), filtered and evaporated under reduced pressure. The residue was purified by pressurized silica gel column chromatography using 93:7 CHCl3 :A, where A=95:5 MeOH:HOAc. 1-Methoxycarbonyl-2-methoxybenzene 4-carboxylic acid was obtained as an oil (30% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665719
Source datasetuspto-grants-1997_09
ORD IDord-b4f68404c43d49ef8cc2bd6d2db573e2
Source noteuspto-grants-1997_09