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HRID 1022848作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Magnesium BromideHCID 82241—
反応物3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazoleHCID 23159812—
反応物Oxalic acid monomethyl ester chlorideHCID 86640482—
反応物HCID 178418306HCID 178418306—
溶媒PentaneHCID 8003—
溶媒TetrahydrofuranHCID 8028—
生成物{4-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-2-methyl-phenyl}-oxo-acetic acid methyl esterHCID 6744429217.8%

反応条件

温度-78 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722673B2
出典データセットuspto-grants-2014_05
ORD IDord-4f0ff100a73a498daab51799e8357975
出典メモuspto-grants-2014_05