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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2220273Erstellt: 27. Oktober 2026

Tetrahydrofuran → [2-(4-Isobutyl-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanol

https://huagongshe.com/reaction/2220273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt{2-[4-Chloro-3-(trifluoromethyl)phenyl]-1,3-benzoxazol-6-yl}methanolHCID 68453052—
EduktHCID 178448254HCID 178448254—
LösungsmittelHydrochloric AcidHCID 313—
Produkt[2-(4-Isobutyl-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanolHCID 68453276—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of [2-(4-chloro-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanol (1 eq) and Pd(PBut3)2 (0.05 eq) is treated with isobutyl zinc bromide in THF (0.5 M, 3 eq). The resulting mixture is heated at 100° C. in microwave for 30 minutes. The reaction mixture is diluted with aqueous HCl (5%) and extracted with EtOAc. The organic solution is washed with brine and dried over Na2SO4. After concentration, the residue is purified by flash column chromatography (30% EtOAc in hexane) to give the desired intermediate [2-(4-isobutyl-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanol. MS: (ES+): 350.1 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07417065B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-7dfa2d220c9e4b939e22386d033ff832
Quellennotizuspto-grants-2008_08