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HRID 1022848Erstellt: 25. Oktober 2026

Ammonium Chloride → {4-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-2-methyl-phenyl}-oxo-acetic acid methyl ester

https://huagongshe.com/reaction/1022848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktMagnesium BromideHCID 82241—
Edukt3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazoleHCID 23159812—
EduktOxalic acid monomethyl ester chlorideHCID 86640482—
EduktHCID 178418306HCID 178418306—
LösungsmittelPentaneHCID 8003—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt{4-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-2-methyl-phenyl}-oxo-acetic acid methyl esterHCID 6744429217,8%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 3-(4-bromo-3-methyl-phenyl)-5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazole (1.00 g) in THF (40 mL) was added tert-butyllithium (16.2 mL of a 1.6 M solution in pentane) at −78° C. After 10 min at this temperature, MgBr2 (0.15 M in THF, 10.3 mL) was added dropwise and left for another 15 min. Oxalic acid methylester chloride (284 mg) was added and the mixture was stirred at −78° C. for 1 h before it was allowed to warm to room temperature over night. Saturated aqueous NH4Cl solution was added and the mixture was extracted with MTBE. The organic layer was separated, dried (Na2SO4) and concentrated in vacuum. The residue was purified by flash chromatography on silica gel to yield the title compound (167 mg, 16%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722673B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-4f0ff100a73a498daab51799e8357975
Quellennotizuspto-grants-2014_05