反応式
[O-]CC.[Na+].[Na].[H][H].[F:8][C:9]([F:20])([F:19])[C:10]1[CH:11]=[C:12]([CH2:16][C:17]#[N:18])[CH:13]=[CH:14][CH:15]=1.[CH3:21][NH:22][CH:23]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:24](OC)=O.[O-]CC.[Na+].C(O)C.[OH2:41]>C(O)C>[CH3:21][N:22]1[C:17]([NH2:18])=[C:16]([C:12]2[CH:13]=[CH:14][CH:15]=[C:10]([C:9]([F:8])([F:19])[F:20])[CH:11]=2)[C:24](=[O:41])[CH:23]1[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1参加物
実験手順
In this example, sodium ethoxide was prepared by mixing 3.0 g of metallic sodium with 100 ml of absolute ethanol. After the evolution of hydrogen stopped, a mixture containing 16.0 g of (3-trifluoromethylphenyl)-acetonitrile and 17.1 g of methyl methylamino-phenylacetate was added dropwise to the sodium ethoxide-ethanol mixture. The resulting mixture was then refluxed overnight (about 16 hours) and then cooled to room temperature. The mixture was then added to 300 ml of water and extracted with diethyl ether. The ethyl ether extract was filtered to remove precipitate. The filtrate was concentrated by evaporation affording a solid. This solid was then triturated in ethyl ether. The ethyl ether was then removed from the solid. The solid was washed several times with ethyl ether and then dried overnight affording 6.2 g of the title compound.
後処理
- temperatureThe resulting mixture was then refluxed overnight (about 16 hours)
- extractionextracted with diethyl ether
- extractionThe ethyl ether extract
- filtrationwas filtered
- customto remove precipitate
- concentrationThe filtrate was concentrated by evaporation
- customaffording a solid
- customThis solid was then triturated in ethyl ether
- customThe ethyl ether was then removed from the solid
- washThe solid was washed several times with ethyl ether
- customdried overnight
出典と根拠
- ORDレコード
- ord-87c51af8ec874c3ea49862dcb3db61f7
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04643762
関連ノート
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