Sodium Cyanide → Benzeneacetonitrile, 2,3-dichloro-
反応式
[Cl:1][C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4]Cl.[C-:11]#[N:12].[Na+]>CS(C)=O.O>[Cl:1][C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][C:11]#[N:12]参加物
5
実験手順
2,3-Dichlorobenzylchloride (5.0 g, 25.5 mmol) was dissolved in 100 ml DMSO. 9.2 g NaCN (188 mmol) were added and the mixture stirred at room temperature for 16 hours. The reaction mixture was diluted with water, and the product extracted with ether. The organic layers were washed with water (2×) and brine, then dried over magnesium sulfate, filtered and concentrated. The product was used as. Crude yield˜quantitative. An analytical sample was purified by column chromatography on silica, using a gradient from 10% to 75% dichloromethane in hexanes as eluent. The combined aqueous layers and wash liquids were treated with 100 ml bleach to oxidize the excess cyanide to less toxic materials.
後処理
- extractionthe product extracted with ether
- washThe organic layers were washed with water (2×) and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customAn analytical sample was purified by column chromatography on silica
- washThe combined aqueous layers and wash liquids
- additionwere treated with 100 ml bleach
出典と根拠
- ORDレコード
- ord-95132224f2204bf5be33c7423de2b104
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08343999B2
反応ノート
読み込み中…