참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenylacetic Acid | HCID 999 | — |
| 반응물 | 4-Fluoroanisole | HCID 9987 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-(5-Fluoro-2-hydroxyphenyl)-2-phenylethanone | HCID 2778585 | 56% |
반응 단계
Phenylacetic acid (8.09 g, 59.46 mmoles) was dissolved in 15 ml dichloromethane. To this mixture, oxalylchloride (5.2 ml, 59.46 mmoles) and DMF (3 drops) were added at 0° C. and stirred for 30 min. The solvent was evaporated and dissolved in 15 ml dichloromethane. To this mixture, 4-fluoroanisole (5.0 g, 39.64 mmoles) was added and cooled to 0° C. At 0° C. AlCl3 (7.92 g, 59.46 mmoles) was added and the reaction mixture was warmed to RT and stirred for 12 h. The reaction mixture was quenched by the addition of 2N HCl, extracted with ethyl acetate, dried over sodium sulphate and concentrated. The crude product was purified by column chromatography with ethyl acetate: petroleum ether to afford the title compound as off-white solid (5.1 g, 56% yield. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 11.43(s,1H), 7.77(dd, J=9.5,3.2 Hz, 1H), 7.42(dt, J=8.7,3.2 Hz, 1H),7.33(t, J=7.3 Hz, 2H), 7.26(m, 3H), 7.01(q, J=4.6 Hz, 1H),4.42(s, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642607B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-b76c0f78a5ef4c369bea9509007d13db |
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| 출처 메모 | uspto-grants-2014_02 |
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