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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111102Generated: October 29, 2026

2,2-Dimethoxyethylmethylamine → ethyl 5-chloro-3-[N-(2,2 dimethoxyethyl)-N methyl(aminomethyl)]-2-benzofurancarboxylate

https://huagongshe.com/reaction/1111102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DimethoxyethylmethylamineHCID 8503—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-bromomethyl-5-chloro-2-benzofurancarboxylateHCID 15678689—
SolventAcetoneHCID 180—
Productethyl 5-chloro-3-[N-(2,2 dimethoxyethyl)-N methyl(aminomethyl)]-2-benzofurancarboxylateHCID 15678690—

Reaction Steps

A mixture of ethyl 3-bromomethyl-5-chloro-2-benzofurancarboxylate (52.75 g, 0.166 mol), methylaminoacetaldehyde dimethyl acetal (19.0 g, 0.167 mol) and potassium carbonate (45 g) in dry acetone (600 ml) was stirred under argon for 30 hours, filtered and the filtrate evaporated. The residue was partitioned between ethyl ether and water and the organic phase was dried with magnesium sulfate, filtered, and concentrated to give ethyl 5-chloro-3-[N-(2,2-dimethoxyethyl)-N-methyl(aminomethyl)]-2-benzofurancarboxylate: mp 58°-60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04978660
Source datasetuspto-grants-1990_12
ORD IDord-8d38d819b1f043fca57ceec45a2a035a
Source noteuspto-grants-1990_12