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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 963789Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/963789

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBromoformHCID 5558—
EduktPotassium HydroxideHCID 14797—
Edukt1,4-DioxaneHCID 31275—
EduktLithium BromideHCID 82050—
Edukt4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-benzaldehydeHCID 18359078—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt[4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]bromoacetic acidHCID 18359186—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05763617
Quelldatensatzuspto-grants-1998_06
ORD IDord-5edfa31d22b64c1f840dff7b614031a6
Quellennotizuspto-grants-1998_06