反应 #417942

ord-a76ba1f3b0ac456bb8cdf65b35c10a73

反应方程式

CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C
bis(pinacolato)diboron
CC(=O)[O-].[K+]
potassium acetate
CCOC(=O)c1ccc(N)c(N)c1
bromide
CCOC(=O)c1ccc(N)c(N)c1
3,4-diamino-benzoic acid ethyl ester
COC(=O)c1ccc(B(O)O)cc1
2
COC(=O)c1ccc(B(O)O)cc1
4-methoxycarbonylphenylboronic acid

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤The organic phase was washed with H2O (20 mL)
  2. 2
    干燥dried over sodium sulfate
  3. 3
    浓缩concentrated in vacuo
  4. 4
    其他The residue was further purified by silica gel column chromatography (haxanes/ethyl acetate=1/4 to 0/1 (v/v))

实验过程

Referring to Scheme 11-1, to a solution of the bromide 1 (2.0 g, 4.2 mmol, prepared according to published conditions) in dioxane (60 mL) was added bis(pinacolato)diboron (4.32 g, 17 mmol), Pd(PPh3)4 (0.49 g, 0.42 mmol) and potassium acetate (2.06 g, 21 mmol) under nitrogen atmosphere. The reaction mixture was stirred at 80° C. for 5 h, and then diluted with ethyl acetate (150 mL). The organic phase was washed with H2O (20 mL), dried over sodium sulfate and concentrated in vacuo. The residue was further purified by silica gel column chromatography (haxanes/ethyl acetate=1/4 to 0/1 (v/v)) to give 2 (1.73 g, 79% yield). LC-MS (ESI): m/z 523.3 (M+H)+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08877707B2uspto-grants-2014_11