Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethylformamide → methyl (4E)-4-phenyl-4-[[4-[(3-phenyl-1,2-oxazol-5-yl)methoxy]phenyl]methoxyimino]butanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-(Chloromethyl)-3-phenylisoxazole | HCID 2764057 | — |
| 반응물 | methyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoate | HCID 10946929 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl acetate hexane | HCID 21226206 | — |
| 생성물 | methyl (4E)-4-phenyl-4-[[4-[(3-phenyl-1,2-oxazol-5-yl)methoxy]phenyl]methoxyimino]butanoate | HCID 11826794 | 68.1% |
반응 단계
A mixture of 5-(chloromethyl)-3-phenylisoxazole (238 mg), methyl E-4-(4-hydroxybenzyloxyimino)-4-phenylbutyrate (350 mg), potassium carbonate (310 mg) and N,N-dimethylformamide (10 ml) was stirred at room temperature for 13 hours. Water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain methyl E-4-phenyl-4-[4-(3-phenyl-5-isoxazolylmethoxy)benzyloxyimino]butyrate (358 mg, yield 62%) as a colorless oil from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06924300B2 |
| 출처 데이터셋 | uspto-grants-2005_08 |
| ORD ID | ord-77d38f8e07bf4c62829df83af7b1bea2 |
| 출처 메모 | uspto-grants-2005_08 |