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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727411Generated: October 25, 2026

Hydrochloric Acid → [4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]bromoacetic acid

https://huagongshe.com/reaction/727411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromoformHCID 5558—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-DioxaneHCID 31275—
ReactantLithium BromideHCID 82050—
Reactant4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-benzaldehydeHCID 18359078—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product[4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]bromoacetic acidHCID 18359186—

Reaction Steps

440 microliters of bromoform were added at -5° C. to a mixture of 4.26 mg of lithium bromide, 598 mg of potassium hydroxide and 5 ml of water and then, a solution of 825 mg of a 4-cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-benzaldehyde (preparation given hereafter) in 5 ml of dioxane was added dropwise. The mixture was stirred for 72 hours at 0° C. to -5° C. and was poured into a stirred mixture at 0° C. to -5° C. of 15 ml of ethyl acetate and 11 ml of hydrochloric acid. Extraction was carried out with ethyl acetate and the extracts were washed, dried and evaporated to dryness under reduced pressure. The oil obtained was used as is for the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712266
Source datasetuspto-grants-1998_01
ORD IDord-86ea1b37963e45928eac0835ff312e2b
Source noteuspto-grants-1998_01