Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1022848생성일: 2026년 10월 26일
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Magnesium Bromide | HCID 82241 | — |
| 반응물 | 3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole | HCID 23159812 | — |
| 반응물 | Oxalic acid monomethyl ester chloride | HCID 86640482 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Pentane | HCID 8003 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | {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% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08722673B2 |
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| 출처 데이터셋 | uspto-grants-2014_05 |
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| ORD ID | ord-4f0ff100a73a498daab51799e8357975 |
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| 출처 메모 | uspto-grants-2014_05 |
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