反应 #1121787

ord-baf15c5a18d049d192379e244c0333ee

反应方程式

O=C(O)c1ccc(F)cc1
4-fluorobenzoic acid
CCN(C(C)C)C(C)C
diisopropylethylamine
On1nnc2ccccc21
HOBT
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HBTU
CNOC.Cl
N,O-dimethyl hydroxylamine hydrochloride
CON(C)C(=O)c1ccc(F)cc1
4-fluoro-N-methoxy-N-methyl-benzamide
收率 79.0%
CON(C)C(=O)c1ccc(F)cc1
4-Fluoro-N-methoxy-N-methyl-benzamide
收率 79.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGAfter stirring at room temperature for 2 hours
  2. 2
    洗涤washed with 4×50 mL of water
  3. 3
    浓缩The combined organic layers is concentrated
  4. 4
    其他purified by flash column chromatography (hexane 70%, EtOAc 30%)

实验过程

To a solution of 4-fluorobenzoic acid (6.8 g, 48.57 mmole) in 100 mL of DMF at room temperature, is added diisopropylethylamine (25.3 mL, 145.7 mmole). After stirring at room temperature for 20 minutes, HOBT (7.22 g, 53.43 mmole), HBTU (20.26 g, 53.43 mmole) and N,O-dimethyl hydroxylamine hydrochloride (5.69 g, 58.29 mmole) are added to the reaction solution. After stirring at room temperature for 2 hours, the reaction solution is diluted with 200 mL of EtOAc and washed with 4×50 mL of water. The combined organic layers is concentrated and purified by flash column chromatography (hexane 70%, EtOAc 30%) to yield 4-fluoro-N-methoxy-N-methyl-benzamide (4a) (7.0 g, yield 79%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08546336B2uspto-grants-2013_10