Dimethylformamide → 4-(Hydroxymethyl)thiophene-2-carbonitrile
反応式
I[C:2]1[S:6][CH:5]=[C:4]([CH2:7][OH:8])[CH:3]=1.[CH3:9][N:10](C=O)C>CCOC(C)=O.[C-]#N.[Zn+2].[C-]#N>[OH:8][CH2:7][C:4]1[CH:3]=[C:2]([C:9]#[N:10])[S:6][CH:5]=1参加物
5
反応条件
- 温度
- 80 °C
実験手順
To a solution of (5-iodo-thiophene-3-yl)methanol (42 g, 176 mmol) in 150 mL of DMF is added zinc cyanide (12.4 g, 106 mmol) and tetrakis(triphenylphospine)palladium (0) (8.13 g, 7.04 mmol). The solution is heated to 80° C. After 6 h, the solution is diluted with 3 L of EtOAc. The resulting solution is washed with 1N NH4OH, H2O and sat. NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with gradient of 20% EtOAc/hexanes to 30% EtOAc/hexanes to afford the title compound (10 g, 72 mmol) as a clear oil.
後処理
- washThe resulting solution is washed with 1N NH4OH, H2O and sat. NaCl
- dry with materialThe organic layer is dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude product is purified by column chromatography
- washeluting with gradient of 20% EtOAc/hexanes to 30% EtOAc/hexanes
出典と根拠
- ORDレコード
- ord-e6dea7c2aa4947e5bcc870d26f4d2244
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05731315
反応ノート
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