참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 2-Bromotoluene | HCID 7236 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 1-Benzylpiperidine-4-carbonitrile | HCID 793383 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | (1-Benzylpiperidin-4-yl)(2-methylphenyl)methanone | HCID 20530712 | — |
반응 단계
To 7 parts of magnesium is added dropwise a solution of 50 parts of 1-bromo-2-methylbenzene in 140 parts of 1,1'-oxybisethane so that the mixture is refluxing. The whole is stirred for 15 minutes at reflux. The Grignard-complex is cooled to 10° C. and there is added dropwise a solution of 36 parts of 1-(phenylmethyl)-4-piperidinecarbonitrile in 70 parts of 1,1'-oxybisethane. Upon completion, stirring is continued for 4 hours at room temperature. The reaction mixture is decomposed with a solution of 40 parts of ammonium chloride in 400 parts of water. The organic phase is separated, dried, filtered and evaporated, yielding 31 parts of (2-methylphenyl) [1-(phenylmethyl)-4-piperidinyl]methanone as an oily residue.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04335127 |
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| 출처 데이터셋 | uspto-grants-1982_06 |
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| ORD ID | ord-a396fa39fa0a4d01b260984bec0b0da4 |
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| 출처 메모 | uspto-grants-1982_06 |
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