참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl isothiocyanate | HCID 11167 | — |
| 반응물 | 2-(4-Chlorophenyl)-3-phenylpropanenitrile | HCID 223564 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-methyl-2-(4-chlorophenyl)-2-cyano-thiopropionamide | HCID 19794675 | 31.4% |
반응 단계
To a 10 ml tetrahydrofuran solution containing 1.00 g (6 mmole) of 4-chlorophenylmethylbenzylcyanide was added a 3.2 ml tetrahydrofuran solution containing 2 M of lithium diisopropylamide at -60° C. After stirring for 30 minutes under the same conditions, a 5 ml tetrahydrofuran solution containing 0.44 g (6 mmol) of methyl isothiocyanate was added to the mixture and the mixture was allowed to stand at room temperature overnight. The solvent was removed from the reaction mixture under reduced pressure and water was added to the residue. The mixture was extracted with 50 ml of ethyl acetate, dried and condensed under reduced pressure, and then purified by silica gel chromatography and recrystallized from hexane to obtain 0.45 g (yield: 31.4 %) of N-methyl-2-(4-chlorophenyl)-2-cyano-thiopropionamide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05246958 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-97a71ab8b30846a79c74a25e489cdea9 |
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| 출처 메모 | uspto-grants-1993_09 |
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