참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-(Chloromethyl)-4-cyanobenzoyl chloride | HCID 11344910 | — |
| 반응물 | Ethyl acetate hexane | HCID 21226206 | — |
| 반응물 | HCID 178418676 | HCID 178418676 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Chloromethyl-4-(4-fluoro-benzoyl)-benzonitrile | HCID 9943434 | — |
반응 단계
A solution of 4-fluoro phenylmagnesium bromide (3.76 g) in tetrahydrofuran (15 ml) was added to a cooled solution of 2-chloromethyl-4-cyano-benzoyl chloride (3.95 g) in tetrahydrofuran (10 ml) so that the temperature did not raise above 0° C. The mixture was warmed slowly to room temperature and stirred over night. Saturated ammonium chloride solution (60 ml) was added and stirring continued for 0.5 hours. The phases were separated and the aqueous phase was extracted with diethylether (30 ml). The combined organic phases were dried over sodium sulfate, filtered and dried in vacuo to give a brown solid. Flash chromatography (ethyl acetate/n-hexane=1/10) provided the product as colourless solid. Yield 2.95 g, 58%. 1H NMR (CDCl3, 400 MHz): 4.71 (2H, s), 7.16-7.21 (2H, m), 7.46 (1H, d, J=7.9 Hz), 7.71 (1H, dd, J=1.5, 7.9 Hz), 7.81-7.86 (2H, m), 7.89 (1H, d, J=1.5 Hz). 13C NMR (CDCl3, 100 MHz): 42.3, 115.0, 116.4, 116.6, 117.9, 129.6, 132.95, 132.98, 133.4, 133.5, 134.3, 138.7, 142.4, 165.5, 168.1, 194.5.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06753433B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-e922eef638ad42aaa2bcc784d588c265 |
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| 출처 메모 | uspto-grants-2004_06 |
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