反応 #45335

ord-bcdbf29868c8476a87c9bbdc191742e7

反応方程式

Nc1cc(CO)cc(C(F)(F)F)c1
[3-amino-5-(trifluoromethyl)phenyl]methanol
CC(C)(C)ON=O
t-butyl nitrite
ICI
CH2I2
OCc1cc(I)cc(C(F)(F)F)c1
[3-iodo-5-(trifluoromethyl)phenyl]methanol

反応条件

温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was maintained at this temperature for 30 minutes
  2. 2
    温度The reaction was then cooled to room temperature
  3. 3
    その他purified with 100% hexanes to 25% EtOAc/hexanes

実験手順

[3-amino-5-(trifluoromethyl)phenyl]methanol (500 mg, 5.2 mmol) was suspended in CH2I2 (5 mL) and t-butyl nitrite (622 μL, 5.2 mmol) was added dropwise by syringe. The reaction was heated slowly to 100° C. and was maintained at this temperature for 30 minutes. The reaction was then cooled to room temperature, diluted with hexanes (50 mL), loaded on a silica gel column, and purified with 100% hexanes to 25% EtOAc/hexanes to afford [3-iodo-5-(trifluoromethyl)phenyl]methanol. Rf=0.19 (15% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.91 (s, 1H), 7.87 (s, 1H), 7.59 (s, 1H), 4.73 (d, J=4.9 Hz, 2H), 1.86 (t, J=5.6 Hz, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07737295B2uspto-grants-2010_06