Tetrabutylammonium Fluoride → 2-Ethynyl-5-(4-methoxyphenyl)pyrazine
反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[N:13][C:12]([C:15]#[C:16][Si](C)(C)C)=[CH:11][N:10]=2)=[CH:5][CH:4]=1.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C(Cl)Cl>[C:15]([C:12]1[CH:11]=[N:10][C:9]([C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)=[CH:14][N:13]=1)#[CH:16]参加物
4
実験手順
To 2.00 g (7.08 mmol) 2-(4-methoxyphenyl)-5-((trimethylsilyl)ethynyl)pyrazine in 50 mL DCM are added 2.08 g (7.44 mmol) TBAF*H2O and the reaction mixture is stirred at r.t. for 30 min. The mixture is washed with 50 mL water (3×) and the organic layer is dried with MgSO4 and the solvent is removed in vacuo. The crude product is purified by column chromatography (silica gel, PE/EtOAc 100/0→80/20).
後処理
- washThe mixture is washed with 50 mL water (3×)
- dry with materialthe organic layer is dried with MgSO4
- customthe solvent is removed in vacuo
- customThe crude product is purified by column chromatography (silica gel, PE/EtOAc 100/0→80/20)
出典と根拠
- ORDレコード
- ord-3a9d6764fffd41d2b09dca3377d4193e
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08835472B2
反応ノート
読み込み中…