HRID132192

反应详情

EQUATION

反应方程式

HRID 132192 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Acetophenone (5.0 mL, 43 mmol) was dissolved in methanol (50 mL). Hydroxylamine hydrochloride (6.1 g, 88 mmol) was added to the mixture followed by 10N sodium hydroxide (10 mL, 100 mmol). Reaction was stirred at room temperature for 20 minutes. 10N Sodium hydroxide (5 mL, 50 mmol) was added to the mixture. Reaction was heated at reflux for 1 hour. Mixture was cooled to room temperature and stirred for 4 hours. Reaction mixture was concentrated in vacuo. Residue was treated with water. Mixture was extracted 2× diethyl ether. Combined extracts were washed 1× water, 1× brine. Organic layer was dried (magnesium sulfate), filtered and concentrated. Title compound was obtained as white solid in 76% yield. MS m/e (M+H)+=136.0.

WORKUP

后处理

  1. customReaction
  2. customReaction
  3. temperaturewas heated
  4. temperatureat reflux for 1 hour
  5. temperatureMixture was cooled to room temperature
  6. stirringstirred for 4 hours
  7. customReaction mixture
  8. concentrationwas concentrated in vacuo
  9. additionResidue was treated with water
  10. extractionMixture was extracted 2× diethyl ether
  11. washCombined extracts were washed 1× water, 1× brine
  12. dry with materialOrganic layer was dried (magnesium sulfate)
  13. filtrationfiltered
  14. concentrationconcentrated