反応 #166060

ord-999fdb07a7264857b0b22f06af7d7172

反応方程式

Cc1ccc(C)cc1
p-xylene
O=C(Cl)c1cc(F)cc(F)c1
3,5-difluorobenzoyl chloride
C=Cc1ccc(OC(C)=O)cc1
4-acetoxystyrene
CN1CCOCC1
N-methyl morpholine
CC(=O)Oc1ccc(C=Cc2cc(F)cc(F)c2)cc1
product
収率 74.4%
CC(=O)Oc1ccc(C=Cc2cc(F)cc(F)c2)cc1
4′-acetoxy-3,5-difluorostilbene
収率 74.4%

溶媒

反応条件

温度
120°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度Then it was cooled to room temperature
  2. 2
    ろ過filtered
  3. 3
    洗浄The filtrate was washed with brine
  4. 4
    乾燥dried over Na2SO4
  5. 5
    ろ過Then it was filtered
  6. 6
    その他purified via flash chromatography

実験手順

A 25 mL round bottom flask was charged with p-xylene (10 mL), Pd(OAc)2 (11.3 mg, 0.05 mmol), 1,3-bis-(2,6-diisopropylphenyl)imidazolinium chloride (21.4 mg, 0.05 mmol), 3,5-difluorobenzoyl chloride (0.89 g, 5 mmol), 4-acetoxystyrene (0.97 g, 6 mmol), and N-methyl morpholine (0.69 g, 6 mmol). The mixture was stirred at 120° C. for 3.5 h under nitrogen atmosphere. Then it was cooled to room temperature and EtOAc was added and filtered. The filtrate was washed with brine and dried over Na2SO4. Then it was filtered and purified via flash chromatography and gave the product (1.02 g, 74%) as white solid. Data are: 1H NMR (CDCl3, 300 MHz) δ 7.51 (d, J=8.4 Hz, 2H), 7.12-6.97 (m, 6H), 6.70 (t, 1H), 2.31 (s, 3H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08841477B2uspto-grants-2014_09