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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1282414Erstellt: 27. Oktober 2026

Hydrochloric Acid → HCID 18424393, Verbindung

https://huagongshe.com/reaction/1282414

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-1-chloro-4-(trifluoromethyl)benzeneHCID 67988—
Edukt1-Fluoro-2-fluoromethyl-3-buten-2-olHCID 18424424—
KatalysatorTetrabutylammonium BromideHCID 74236—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylacetamideHCID 31374—
ProduktHCID 18424393HCID 1842439388%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 3-bromo-4-chlorobenzotrifluoride (1.50 g), 1-fluoro-2-fluoromethyl-3-buten-2-ol (0.80 g), potassium carbonate (2.10 g), tetrabutylammonium bromide (325 mg), palladium acetate (56 mg) and N,N-dimethylacetamide (10 ml) was stirred under a nitrogen atmosphere at 80° C. for 14 hours. To the reaction mixture, 1 N HCl was added followed by extraction with a hexane/ethyl acetate mixed (1/1) solvent; the resulting organic layers were combined and washed with a saturated aqueous solution of sodium thiosulfate and a saturated aqueous solution of sodium chloride; the mixture was dried with anhydrous sodium sulfate and concentrated under reduced pressure; the resulting residue was subjected to silica gel column chromatography (eluent; hexane/ethyl acetate=10/1) to give 4-(2-chloro-5-trifluoromethylphenyl)-1-fluoro-2-fluoromethyl-3-trans-buten-2-ol (1.53 g) having a melting point of 61-62° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06455708B1
Quelldatensatzuspto-grants-2002_09
ORD IDord-745a1a71b5384500b36d56cf9bbe7072
Quellennotizuspto-grants-2002_09