反应 #742278

ord-b2fe6831fb734c919a3f468d16151cf9

反应方程式

COc1ccc(NN)cc1
(4-methoxyphenyl)hydrazine
CC(=O)C(C)C
3-methylbutan-2-one
COc1ccc2c(c1)C(C)(C)C(C)=N2
5-methoxy-2,3,3-trimethyl-3H-indole
收率 45.4%

溶剂

反应条件

温度
100°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The mixture was concentrated
  2. 2
    workup.ADDITION1N NaOH was added until pH 9 to 10
  3. 3
    萃取The aqueous solution was extracted with ethyl acetate (50 mL×3)
  4. 4
    干燥The combined organic layers were dried over Na2SO4
  5. 5
    过滤After filtration and concentration
  6. 6
    其他the residue was purified by flash column chromatography

实验过程

A mixture of (4-methoxyphenyl)hydrazine (0.98 g, 7.1 mmol) and 3-methylbutan-2-one (1.53 g, 17.8 mmol) in 20 mL of HOAc was heated at 100° C. overnight. The mixture was concentrated and 1N NaOH was added until pH 9 to 10. The aqueous solution was extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over Na2SO4. After filtration and concentration, the residue was purified by flash column chromatography to give 610 mg of 5-methoxy-2,3,3-trimethyl-3H-indole (45%). 1H NMR (CDCl3) δppm: 7.43 (dd, 1H), 6.81 (m, 2H), 3.83 (s, 3H), 2.26 (s, 3H), 1.28 (s, 6H). LC-MS (M+H): 190.16

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08071388B2uspto-grants-2011_12