HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Magnesium Bromide | HCID 82241 | — |
| Edukt | 3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole | HCID 23159812 | — |
| Edukt | Oxalic acid monomethyl ester chloride | HCID 86640482 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | {4-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-2-methyl-phenyl}-oxo-acetic acid methyl ester | HCID 67444292 | 17,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08722673B2 |
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| Quelldatensatz | uspto-grants-2014_05 |
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| ORD ID | ord-4f0ff100a73a498daab51799e8357975 |
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| Quellennotiz | uspto-grants-2014_05 |
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