참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | n-Butyl lithium | HCID 61028 | — |
| 반응물 | 2,4-Dichlorobenzonitrile | HCID 81050 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Amino-3-(2,4-dichlorophenyl)acrylonitrile | HCID 66911322 | — |
반응 단계
Under argon, 90 g (889.46 mmol) of diisopropylamine were initially charged in 1660 ml of THF at −70° C. in a three-necked flask with mechanical stirrer. 124.66 ml of N-butyllithium solution (2.5 M in hexane, 758.66 mmol) were added dropwise at such a rate that the temperature did not exceed −60° C. The mixture was stirred for 10 min, and a solution of 32.22 g (784.82 mmol) of acetonitrile in 340 ml of THF was then slowly added dropwise and the suspension was stirred for 30 min. A solution of 90 g (523.21 mmol) of 2,4-dichlorobenzonitrile in 340 ml of THF was then added dropwise, and the mixture was stirred at −70° C. for 20 min. The mixture was allowed to slowly warm to RT and stirred at RT for a further 16 h. 600 ml of water were added, most of the THF was distilled off and water and dichloromethane were added. The organic phase was washed with saturated aqueous sodium chloride solution. Removal of the solvent gave crystals which were purified by trituration with diethyl ether. This gave 76.5 g (69% of theory) of the product as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08436003B2 |
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| 출처 데이터셋 | uspto-grants-2013_05 |
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| ORD ID | ord-cebb1e0ed83a4ba4b6d18e0e701c5e20 |
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| 출처 메모 | uspto-grants-2013_05 |
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