تفاعل #710525

ord-912cce266b374c0486508762668d0a39

معادلة التفاعل

C=CCBr
Allyl bromide
Oc1ccccc1O
pyrocatechol
Oc1ccccc1O
Compound A
Oc1ccccc1O
pyrocatechol
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(C)=O
acetone
C=CCc1ccc(O)c(O)c1CC=C
3,4-diallylbenzene-1,2-diol

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
177.5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITThe stirring was continued for another hour
  2. 2
    درجة الحرارةthe mixture was refluxed for 5 hours
  3. 3
    أخرىAfter completion of the reaction
  4. 4
    ترشيحthe solid was filtered
  5. 5
    تركيزfiltrate was concentrated
  6. 6
    استخلاصextracted with chloroform (3×50 mL)
  7. 7
    غسيلwashed with brine (1×50 mL)
  8. 8
    تجفيفdried over anhydrous sodium sulfate and solvent
  9. 9
    أخرىwas removed under reduced pressure
  10. 10
    أخرىThe reaction mixture was purified by column chromatography (silica gel: 60-120 mesh)
  11. 11
    درجة الحرارةwith increasing concentration of chloroform
  12. 12
    غسيلElution of 60% and 75% chloroform in petroleum ether yielded pure compounds corresponding to Compound No

الإجراء التجريبي

To a solution of pyrocatechol (Compound A) (1 g, 0.009 mol) and dry acetone (10 mL) was added dry K2CO3 (2.646 g, 0.0189 mol) in portions for 30 minutes. The stirring was continued for another hour. Allyl bromide (1.6 mL, 0.0189 mol) was added to the mixture for 30 minutes and the mixture was refluxed for 5 hours. After completion of the reaction, the solid was filtered and filtrate was concentrated and extracted with chloroform (3×50 mL), washed with brine (1×50 mL), dried over anhydrous sodium sulfate and solvent was removed under reduced pressure. The crude material was heated at 175-180° C. for 2 hours. The reaction mixture was purified by column chromatography (silica gel: 60-120 mesh) using petroleum ether with increasing concentration of chloroform. Elution of 60% and 75% chloroform in petroleum ether yielded pure compounds corresponding to Compound No. 2 and Compound No. 3 as liquids respectively.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09302967B2uspto-grants-2016_04