참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-(4-Hydroxyphenyl)propionic acid | HCID 10394 | — |
| 반응물 | 2-Bromo-1,2-diphenylethan-1-one | HCID 102630 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 촉매 | Sulfuric Acid | HCID 1118 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-[2-(4,5-Diphenyl-2-oxazolyl)ethyl]phenol | HCID 19783623 | 65.1% |
반응 단계
Sodium metal (1.00 g, 43 mg atom) was dissolved in ethanol (125 mL) and 3-(4-hydroxyphenyl)propionic acid (6.04 g, 36 mmol) added to give a white precipitate. The mixture was warmed briefly with stirring and concentrated H2SO4 (3 drops) added followed by 2-bromo-2-phenylacetophenone (1.00 g, 36 mmol). The mixture was heated at reflux for 2 hours, cooled, concentrated and diluted with water. The mixture was extracted with CH2Cl2, the combined extracts dried over sodium sulfate and concentrated to give an oil which was dissolved in acetic acid (250 mL). Ammonium acetate (14.00 g, 180 mmol) was added and the mixture heated to reflux. After 100 minutes, the solution was cooled, diluted with water and extracted with CH2Cl2. The combined extracts were dried over sodium sulfate and the solvent evaporated to leave a solid that was triturated with a mixture of hexanes and diethyl ether and filtered to give 4-[2 -(4,5-diphenyl-2-oxazolyl)ethyl]phenol (8.00 g, 64%). An analytical sample was prepared by recrystallizing 1.5 g from a mixture of hexanes and CH2Cl2 to give 1.20 g of pure material, m.p. 142°-144° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05262540 |
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| 출처 데이터셋 | uspto-grants-1993_11 |
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| ORD ID | ord-5ed5493abe86493caa1b6c377111fbeb |
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| 출처 메모 | uspto-grants-1993_11 |
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