反応式
[NH2:1][C:2]1[C:7]([I:8])=[CH:6][C:5]([Br:9])=[CH:4][C:3]=1[S:10]([OH:13])(=O)=[O:11].C(N(CCCC)CCCC)CCC.[Cl:27]P(Cl)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>ClCCl>[NH2:1][C:2]1[C:7]([I:8])=[CH:6][C:5]([Br:9])=[CH:4][C:3]=1[S:10]([Cl:27])(=[O:13])=[O:11]参加物
5
実験手順
To a solution containing 7.6 g (20 mmol) of 2-amino-5-bromo-3-iodobenzenesulphonic acid and 4.8 ml (20 mmol) of tributylamine in 20 ml of dichloromethane is added dropwise, at 0° C. under a nitrogen atmosphere, a solution of dichlorotriphenylphosphorane (9.7 g (37.5 mmol) in 45 ml of dichloromethane). The mixture is brought to room temperature, stirring is continued for 18 hours and the product is purified by chromatography on a column of silica gel, eluting with a dichloromethane/pentane mixture (2:8).
後処理
- additionis added dropwise, at 0° C. under a nitrogen atmosphere
- customis brought to room temperature
- customthe product is purified by chromatography on a column of silica gel
- washeluting with a dichloromethane/pentane mixture (2:8)
出典と根拠
- ORDレコード
- ord-88dddb4a2a8f4aa2883165c8ba4e3fc3
- 出典データセット
- uspto-grants-1998_01
- 特許番号
- US05712393
関連ノート
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