反応式
[CH:1](=O)[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.[C-:8]#[N:9].[Na+].[NH4+:11].[Cl-].N.CO.N>CO>[NH2:11][CH:1]([C:8]#[N:9])[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1参加物
7
実験手順
Furfural (1.0 equiv) is mixed with NaCN (1.1 equiv) and NH4Cl (1.1 equiv) in 2 Molar NH3/MeOH (4 equiv NH3). The flask is fitted with a reflux condenser and mixture is refluxed. At the end of each of the first 3 h an additional equivalent of NH3 in MeOH is added. The reaction mixture is cooled and the excess solids are filtered away on a frit. The filtrate is concentrated by rotary evaporation and the residue is triturated with diethyl ether and the mixture is filtered again. The filtrate is concentrated on a rotovap. The product is purified, if necessary, by flash chromatography on silica gel with EtOAc/hexanes as an eluent to yield amino-cyano-(furan-2-yl)methane.
後処理
- customThe flask is fitted with a reflux condenser
- temperaturemixture is refluxed
- temperatureThe reaction mixture is cooled
- filtrationthe excess solids are filtered away on a frit
- concentrationThe filtrate is concentrated by rotary evaporation
- customthe residue is triturated with diethyl ether
- filtrationthe mixture is filtered again
- concentrationThe filtrate is concentrated on a rotovap
- customThe product is purified
出典と根拠
- ORDレコード
- ord-b2d95a6cab124d4493b35da172c7f5e9
- 出典データセット
- uspto-grants-2005_08
- 特許番号
- US06936606B2
関連ノート
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