HRID1372511

反应详情

EQUATION

反应方程式

HRID 1372511 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

The diketone from step 1 (0.6 g, 2.14 mmol) was dissolved in toluene (15 mL) and treated with acetic acid (0.236 mL, 4.12 mmol) and pyrrolidine (0.344 mL, 4.12 mmol). The resulting solution was stirred and heated in an oil bath at 100° C. for 1.5 hours. After cooling to room temperature, the mixture was filtered through a pad of silica gel and the product was washed off with EtOAc. The filtrate and washings were concentrated under vacuum. The residue was purified by flash chromatography on a Biotage 40M KP-Sil column, eluting with 4:1 to 3:1 hexanes-EtOAc. The product containing fractions were evaporated under vacuum to provide 7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-one (0.45 g, 80%) as a yellow solid.

WORKUP

后处理

  1. temperatureAfter cooling to room temperature
  2. filtrationthe mixture was filtered through a pad of silica gel
  3. washthe product was washed off with EtOAc
  4. concentrationThe filtrate and washings were concentrated under vacuum
  5. customThe residue was purified by flash chromatography on a Biotage 40M KP-Sil column
  6. washeluting with 4:1 to 3:1 hexanes-EtOAc
  7. additionThe product containing fractions
  8. customwere evaporated under vacuum