반응 #1435698

ord-206c9e4dcfc6488eaaeb75ef2f933b50

반응 방정식

Cc1cc(=O)n(-c2ccccc2)[nH]1
3-Methyl-1-phenylpyrazol-5-one
[Ca+2].[OH-].[OH-]
calcium hydroxide
CC(C)(C)CC(=O)Cl
tert-butylacetyl chloride
Cc1[nH]n(-c2ccccc2)c(=O)c1C(C)(C)C
4-tert-Butyl-3-methyl-1-phenylpyrazol-5-one

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타equipped with a stirrer
  2. 2
    온도reflux condenser
  3. 3
    기타Dry
  4. 4
    workup.DISTILLATIONdistilled dioxane (40 ml)
  5. 5
    workup.ADDITIONwas added
  6. 6
    workup.ADDITIONwas added
  7. 7
    온도The mixture was heated
  8. 8
    온도to reflux for 4 hours
  9. 9
    기타A light brown precipitate formed immediately
  10. 10
    여과which was filtered off under suction
  11. 11
    세척The product was washed with water
  12. 12
    기타dried under vacuum at 50° C
  13. 13
    기타The product was recrystallised from methanol
  14. 14
    기타to give an off-white crystalline solid, m.p 85–86° C.

실험 절차

3-Methyl-1-phenylpyrazol-5-one (5 g; 0.029 mole) was placed in a flask equipped with a stirrer and reflux condenser. Dry and distilled dioxane (40 ml) was added by warming and to the clear solution calcium hydroxide (6.4 g; 0.086 mole) was added followed by drop wise addition of tert-butylacetyl chloride (4.8 ml; 0.034 mole). The mixture was heated to reflux for 4 hours and then poured into 2M HCl (200 ml) to decompose the calcium complex. A light brown precipitate formed immediately, which was filtered off under suction after refrigerating overnight. The product was washed with water and dried under vacuum at 50° C. The product was recrystallised from methanol to give an off-white crystalline solid, m.p 85–86° C.; 6.8 g (82%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07211334B2uspto-grants-2007_05