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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845692Generated: October 27, 2026

Potassium Carbonate → 2-(4-benzyloxyphenoxy)propionic acid N-cyano-N-methylamide

https://huagongshe.com/reaction/845692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromopropionic acid N-cyano-N-methylamideHCID 53744792—
Reactant2-[2-[[2-(2,5-Dihydroxyphenyl)phenyl]methoxymethyl]phenyl]benzene-1,4-diolHCID 131711022—
SolventDimethylformamideHCID 6228—
Product2-(4-benzyloxyphenoxy)propionic acid N-cyano-N-methylamideHCID 5452635163%

Reaction Steps

With efficient stirring, B 19.1 g (0.1 mole) of 2-bromopropionic acid N-cyano-N-methylamide are added dropwise to a solution of 20.0 g (0.1 mole) of hydroquinone monobenzyl ether and 16.5 g (0.12 mole) of potassium carbonate in 200 ml of dimethylformamide. After the slightly exothermic reaction has subsided, the reaction mixture is heated for 3 hours to 40° C. The precipitated salts are then removed by filtration and the filtrate is concentrated by evaporation. The residue is dissolved in ether and the ether solution is extracted with dilute sodium hydroxide solution. The organic phase is dried over sodium sulfate, the solvent is evaporated off and the residue is distilled in vacuo, affording 19.5 g (63% of theory) of 2-(4-benzyloxyphenoxy)propionic acid N-cyano-N-methylamide with a melting point of 56°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04759796
Source datasetuspto-grants-1988_07
ORD IDord-b8a4e543e28e4193a37b5632288dddc1
Source noteuspto-grants-1988_07