반응 #93556

ord-70011b4f8d694016b0837d15af9bff3c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타fitted with a borosilicate glass
  2. 2
    여과filter
  3. 3
    기타after degassing for 1 hour under nitrogen
  4. 4
    추출The photolysis mixture was extracted with 0.25N NaOH
  5. 5
    세척washed with ether
  6. 6
    추출extracted with chloroform
  7. 7
    건조The chloroform was dried over anhydrous MgSO4
  8. 8
    기타to give a crude yellow solid
  9. 9
    기타the combined crude product from these reactions was chromatographed through silica gel (0.063-0.2 mm)
  10. 10
    기타The solid obtained from the chromatography
  11. 11
    기타was recrystallized from benzene

실험 절차

A solution of 7.00 g (0.042 mol) of 2-diazo-5,5-dimethylcyclohexane-1,3-dione in 300 ml of 5-t-butyl-m-xylene and 250 ml chlorobenzene containing 38.38 g (0.21 mol) of benzophenone was irradiated overnight with a 200 watt mercury arc lamp fitted with a borosilicate glass filter after degassing for 1 hour under nitrogen. The photolysis mixture was extracted with 0.25N NaOH, washed with ether, acidified with 1N HCl, and extracted with chloroform. The chloroform was dried over anhydrous MgSO4 and stripped to give a crude yellow solid. The photolysis was repeated and the combined crude product from these reactions was chromatographed through silica gel (0.063-0.2 mm) using benzene-ethyl acetate. The solid obtained from the chromatography was recrystallized from benzene to give 2.76 g (11%) of 2-(2',6'-dimethyl-4'-t-butylphenyl)-5,5-dimethyl-1,3-cyclohexanedione as white crystals, mp 244°-49° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04613617uspto-grants-1986_09