HRID490857

反应详情

EQUATION

反应方程式

HRID 490857 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a mixture of perfluorobenzoyl chloride (2.51 g, 10.9 mmol) and 2-bromothiophene (1.86 g, 11.4 mmol) in carbon disulfide (80 mL), aluminum chloride (2.90 g, 21.8 mmol) was added in portions over 10 min with vigorous mechanical stirring. The reaction mixture turned red and was stirred for 2.5 h before being quenched with water (80 mL). The organics were then separated, the aqueous layer extracted with carbon disulfide (3×50 mL), and the combined organics washed with water (3×100 mL) and dried over MgSO4. After filtration, the organics were concentrated in vacuo and the chromatographed on a silica gel column (hexane:ether=9:1) to yield 1.23 g (32%) green crystals. mp 51-54° C.; 1H NMR (DMSO): δ 7.78 (d, 2H, 3J=3.6 Hz), 7.54 (d, 2H, 3J=4.4 Hz); 19F NMR (DMSO): δ −142.1 (m, 2H), −151.6 (m, 1H), −160.6 (m, 2H) Anal. Calcd for C11H2BrF5OS: C 37.00, H 0.56. Found: C 37.37, H 0.83; MS (EI): m/z (%) 355.8 (92) [M+].

WORKUP

后处理

  1. additionwas added in portions over 10 min with vigorous mechanical stirring
  2. custombefore being quenched with water (80 mL)
  3. customThe organics were then separated
  4. extractionthe aqueous layer extracted with carbon disulfide (3×50 mL)
  5. washthe combined organics washed with water (3×100 mL)
  6. dry with materialdried over MgSO4
  7. filtrationAfter filtration
  8. concentrationthe organics were concentrated in vacuo
  9. customthe chromatographed on a silica gel column (hexane:ether=9:1)