Ammonium Chloride → 4-Bromo-7-(1-methylethyl)-1H-indole
反応式
[CH:1]([Mg]Br)=[CH2:2].[Br:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:14])[CH3:13])=[C:8]([N+:15]([O-])=O)[CH:7]=1.[NH4+].[Cl-]>C1COCC1>[Br:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:14])[CH3:13])=[C:8]2[C:7]=1[CH:1]=[CH:2][NH:15]2参加物
5
実験手順
Vinyl magnesium bromide (1 M in THF) (98 mL, 98 mmol) was added to 4-bromo-1-isopropyl-2-nitrobenzene (4 g, 16.39 mmol) in THF (60 mL) at −40° C. The reaction mixture was stirred for 1 h, then poured into saturated aqueous NH4Cl and extracted with ether. The combined ethereal extracts were dried (MgSO4) and concentrated. Chromatography over silica eluting with 1-20% EtOAc/hexanes afforded the title compound. LC-MS: calculated for C11H12BrN 237,02, observed m/e 238.2 (M+H)+ Rt (1.96/4 min.).
後処理
- extractionextracted with ether
- dry with materialThe combined ethereal extracts were dried (MgSO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-6ff560a2b9634095b808b0c949ba0a75
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08410284B2
反応ノート
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