Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2221616생성일: 2026년 10월 26일
Dimethylformamide → 5-[2-(4-Hydroxyphenyl)ethyl]-4-methoxymethoxymethyl-2-phenyl-1,3-oxazole
https://huagongshe.com/reaction/2221616
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | [4-(Benzyloxy)benzyl](triphenyl)phosphonium chloride | HCID 383834 | — |
| 반응물 | 4-[(Methoxymethoxy)methyl]-2-phenyl-1,3-oxazole-5-carbaldehyde | HCID 11459274 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-[2-(4-Hydroxyphenyl)ethyl]-4-methoxymethoxymethyl-2-phenyl-1,3-oxazole | HCID 22930724 | 79% |
반응 단계
A mixture of 4-methoxymethoxymethyl-2-phenyl-1,3-oxazole-5-carbaldehyde (3.00 g), 4-benzyloxybenzyltriphenylphosphonium chloride (6.58 g), potassium carbonate (1.84 g) and N,N-dimethylformamide (50 mL) was stirred at room temperature for 15 hrs. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The organic layer was washed successively with dilute hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give a colorless oil from a fraction eluted with ethyl acetate-hexane (1:4, v/v). A mixture of the obtained colorless oil, 5% palladium on carbon (5.00 g) and tetrahydrofuran (200 mL) was stirred under a hydrogen atmosphere at room temperature for 3 hrs. After removing palladium on carbon by filtration, the filtrate was concentrated. The obtained crystals were collected by filtration to give 5-[2-(4-hydroxyphenyl)ethyl]-4-methoxymethoxymethyl-2-phenyl-1,3-oxazole (3.24 g, yield 79%). The crystals were recrystallized from ethyl acetate-hexane. melting point: 102-103° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07368578B2 |
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| 출처 데이터셋 | uspto-grants-2008_05 |
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| ORD ID | ord-ed9fc8cbe28d4a42af490c6b28ee7a01 |
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| 출처 메모 | uspto-grants-2008_05 |
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