HRID1174432

反应详情

EQUATION

反应方程式

HRID 1174432 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

Into a 500 mL 3-neck flask fitted with condenser, addition funnel and a thermometer was added 10.0 g of 2-Amino-4-tert-butylphenol (Aldrich) dissolved in 50.0 mL acetic acid. To the solution was added 3.90 g of 4-(t-butyl)-2-nitrophenol (Aldrich) and 100 mL of concentrated HCl. The contents of the flask were heated to 80° C. by means of an oil bath. Acrolein (Aldrich) (6.78 g) was added over 30 min via the addition funnel. After the addition was complete, the solution was heated to 130° C. for 16 hrs. The solution was allowed to cool to room temperature and then poured into 300 mL cold water and neutralized to pH7.0 by addition of a 25% NaOH solution. A tan precipitate formed which was extracted from the aqueous solution (3×200 ml methylene chloride). The combined extracts were dried with MgSO4 and concentrated to an oil. The oil was resuspended in methylene chloride and the insoluble materials (unreacted 2-amino-4-tert-butylphenol) filtered off. The filtrate was concentrated to an oil and purified by chromatography on silica gel column eluting with 1:1 chloroform:hexanes to remove the non-polar impurities followed by chloroform to elute the product. The product containing fractions were combined and concentrated to an oil which solidified upon standing. Yield 1.56 g (13%)

WORKUP

后处理

  1. customInto a 500 mL 3-neck flask fitted with condenser, addition funnel
  2. additionAfter the addition
  3. temperaturethe solution was heated to 130° C. for 16 hrs
  4. temperatureto cool to room temperature
  5. customA tan precipitate formed which
  6. extractionwas extracted from the aqueous solution (3×200 ml methylene chloride)
  7. dry with materialThe combined extracts were dried with MgSO4
  8. concentrationconcentrated to an oil
  9. filtrationthe insoluble materials (unreacted 2-amino-4-tert-butylphenol) filtered off
  10. concentrationThe filtrate was concentrated to an oil
  11. custompurified by chromatography on silica gel column
  12. washeluting with 1:1 chloroform
  13. customhexanes to remove the non-polar impurities
  14. washto elute the product
  15. additionThe product containing fractions
  16. concentrationconcentrated to an oil which