Carbon tetrabromide → 4-(Bromomethyl)benzene-1,2-dicarbonitrile
反応式
O[CH2:2][C:3]1[CH:4]=[C:5]([C:11]#[N:12])[C:6](=[CH:9][CH:10]=1)[C:7]#[N:8].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C(Br)(Br)(Br)[Br:33]>C1COCC1>[Br:33][CH2:2][C:3]1[CH:4]=[C:5]([C:11]#[N:12])[C:6](=[CH:9][CH:10]=1)[C:7]#[N:8]参加物
5
実験手順
4-Hydroxymethyl-phthalonitrile from step 2 (1.3 g, 8.2 mmol) was dissolved in THF (41 ml) and treated with Ph3P (3.2 g, 12.3 mmol) followed by CBr4 (4 g, 12.3 mmol). The reaction mixture was stirred at room temp. for 21 hours. The solvent was removed in vacuo and the residue purified by flash chromatography (15% EtOAc/Hexane) to yield the desired product.
後処理
- customThe solvent was removed in vacuo
- customthe residue purified by flash chromatography (15% EtOAc/Hexane)
出典と根拠
- ORDレコード
- ord-ca0e1821c093492cbc3d6d390b3e346d
- 出典データセット
- uspto-grants-2000_06
- 特許番号
- US06077853
反応ノート
読み込み中…