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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 974997Erstellt: 24. Oktober 2026

Hydrochloric Acid → 4-(4-Fluorophenyl)but-3-enoic acid

https://huagongshe.com/de/reaction/974997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-FluorobenzaldehydeHCID 68023—
Edukt(2-Carboxyethyl)triphenylphosphonium chlorideHCID 10270534—
EduktPotassium tert-butoxideHCID 23665647—
EduktHCID 178418361HCID 178418361—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(4-Fluorophenyl)but-3-enoic acidHCID 1039738550%

Reaktionsschritte

74.4 g of 4-fluorobenzaldehyde and 233.6 g of β-carboxyethyl-triphenyl phosphonium chloride were suspended in 700 ml of tetrahydrofuran and these were incubated on ice and stirred. Into this 500 ml tetrahydrofuran solution of 141.4 g of potassium tert-butoxide was added slowly dropwise. 30 minutes after temperature was brought to room temperature and then they were stirred for 10 hours. After adding thereto ice water and cleaning with ether, the hydrogen-ion concentration of water layer was set to pH2 with undiluted hydrochloric acid. Extraction was then made with ethyl acetate. After drying with magnesium sulfate and concentration made under reduced pressure, the solid obtained was recrystallized from hydrous ethanol, and 53.98 g of marked compound (yield: 50%) was obtained as white needle crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05607953
Quelldatensatzuspto-grants-1997_03
ORD IDord-1ed36f677c7944f586fef193ca317de3
Quellennotizuspto-grants-1997_03