참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thiophenol | HCID 7969 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | o-Fluorobenzaldehyde | HCID 67970 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(Phenylthio)benzaldehyde | HCID 12340685 | 71.3% |
반응 단계
2-fluoro-benzaldehyde (2.00 g, 16.1 mmol), potassium carbonate (2.45 g, 17.7 mmol) and thiophenol (17.1 mmol) were dissolved in 10.0 mL DMF in a 50 mL round-bottomed flask under dry nitrogen, topped with a reflux condenser. The reaction mixture was heated to 80° C. for 24 hrs. After cooling, the mixture was added to 50 mL of saturated potassium carbonate solution and extracted with 3×50 mL portions of ether. The extracts were dried with magnesium sulfate and evaporated. The crude product was further purified by chromatography on silica gel using 9:1 petroleum ether 60-80 and dichloromethane as eluent to give a yellow oil (2.46 g, 71%). 1H NMR (200 MHz, CDCl3): δ 7.07 (dd, J1=7.8, J2=1.2, 1H), 7.27-7.45 (m, 7H), 7.87 (dd, J1=7.3, J2=2.0, 1H), 10.37 (s, 1H) ppm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08513151B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-b6b53b2b820b49fd899f16bc3caa05a2 |
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| 출처 메모 | uspto-grants-2013_08 |
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