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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361021Generated: October 28, 2026

Hydrochloric Acid → Methyl 4-(cyanomethoxy)benzoate

https://huagongshe.com/reaction/1361021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantMethylparabenHCID 7456—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductMethyl 4-(cyanomethoxy)benzoateHCID 594916—

Reaction Steps

To a mixture of methyl 4-hydroxybenzoate (30.0 g, 0.20 mol), sodium iodide (30.0 g, 0.20 mol) and potassium carbonate (27.6 g, 0.20 mol) in acetone (2000 mL) was added chloroacetonitrile (14.9 g, 0.20 mol). The mixture was stirred at RT for 3 days. Water was added and the mixture was acidified with 1N hydrochloric acid and the mixture was extracted with diethyl ether. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in acetone and chloroacetonitrile (6.04 g, 0.08 mol), sodium iodide (12.0 g, 0.08 mol) and potassium carbonate (11.1 g, 0.08 mol) were added and the mixture was stirred for 16 hours at RT and at 60° C. More chloroacetonitrile was added until the conversion was 97%. Water was added and the mixture was acidified with 1N hydrochloric acid and the mixture was extracted with diethyl ether. The combined organic layers were dried over Na2SO4 and concentrated in vacuo to afford methyl 4-cyanomethyloxybenzoate in quantitative yield. This compound was used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-a30bb249df2e425ea668342edb258337
Source noteuspto-grants-2011_02