反応式
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]2[N:8]=[CH:9][S:10][C:6]=2[CH:5]=1)([O-:3])=[O:2].C[Mg+].[Br-].[CH:16](Cl)(Cl)Cl>C1COCC1>[CH3:16][C:5]1[C:6]2[S:10][CH:9]=[N:8][C:7]=2[CH:11]=[CH:12][C:4]=1[N+:1]([O-:3])=[O:2]参加物
5
実験手順
To a solution of 6-nitrobenzothiazole (1.4 g, 7.7 mmol) in 50 mL of THF was added 5.1 mL of MeMgBr (15.3 mmol) dropwise in 0.5 h period at 0° C. The reaction mixture was then stirred for additional 2 h. It was quenched by adding THF solution of 2,3-dichloro-5,6-dicyanobenzoquinone until the color of the solution turns to dark green. The reaction mixture was concentrated in vacuo to yield a dark solid which was subjected to column chromatography (CHCl3, neat) to provide 0.68 g (3.5 mmol, 46%) of the desired product.
後処理
- customIt was quenched
- additionby adding THF solution of 2,3-dichloro-5,6-dicyanobenzoquinone until the color of the solution
- concentrationThe reaction mixture was concentrated in vacuo
- customto yield a dark solid which
出典と根拠
- ORDレコード
- ord-3121030d55ca48b4b5ba553ac7b0a977
- 出典データセット
- uspto-grants-2001_10
- 特許番号
- US06303643B1
関連ノート
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