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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515654Generated: October 30, 2026

Water → Methyl 4-(MethoxyMethyl)benzoate

https://huagongshe.com/reaction/515654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant4-(methoxymethyl)benzoic acidHCID 308473—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductMethyl 4-(MethoxyMethyl)benzoateHCID 15247548—

Reaction Steps

Methyl 4-(methoxymethyl)benzenecarboxylate (MMBC) was prepared from 4-(methoxymethyl)benzoic acid (Sigma-Aldrich) by esterification in methanol using HCl as catalyst. The reaction was conducted under reflux conditions for 2.5 hours. Following the reaction, water and ethyl acetate was added and the MMBC product was separated using liquid extraction into the ethyl acetate phase. The ethyl acetate was then removed by rotary evaporation to obtain the isolated MMBC product. The 1H NMR spectrum of the product was collected in CDCl3, and the peak positions and integrated areas matched that of the reported 1H NMR spectrum for this molecule.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108979B2
Source datasetuspto-grants-2015_08
ORD IDord-48f7b8576704440982bdfc6697610562
Source noteuspto-grants-2015_08