تفاعل #1596973

ord-9f45caefc9094fa28cf0559b401885ee

معادلة التفاعل

O=C(O)c1ccc(O)cc1
p-hydroxybenzoic acid
C=CCCCCCCBr
8-bromo-1-octene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)N(C)C
N,N-dimethylacetamide
C=CCCCCCCOc1ccc(C(=O)O)cc1
4-(7-octenyloxy)-benzoic acid

المذيبات

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooled
  2. 2
    استخلاصextracted with ethyl acetate (500 mL)
  3. 3
    غسيلwashed two times with water (100 mL)
  4. 4
    تجفيفThis was dried with anhydrous magnesium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىThe solvent was removed through concentration under reduced pressure
  7. 7
    workup.DISSOLUTIONthe residue was dissolved in methanol (100 mL)
  8. 8
    workup.ADDITIONgradually added
  9. 9
    درجة الحرارةheated
  10. 10
    درجة الحرارةunder reflux for 2 hours
  11. 11
    درجة الحرارةAfter cooled
  12. 12
    ترشيحthe formed crystal was collected through filtration
  13. 13
    غسيلwashed with water
  14. 14
    أخرىThis was dried
  15. 15
    أخرىto give TP-5C (63.3 g, 85%)

الإجراء التجريبي

p-hydroxybenzoic acid (33.2 g), 8-bromo-1-octene (57.3 g), potassium carbonate (41.5 g) and N,N-dimethylacetamide (200 mL) were put into a 500-mL three-neck flask, and stirred at 120° C. for 5 hours. After cooled, the reaction mixture was poured into water (200 mL), extracted with ethyl acetate (500 mL), and washed two times with water (100 mL). This was dried with anhydrous magnesium sulfate and then filtered. The solvent was removed through concentration under reduced pressure, the residue was dissolved in methanol (100 mL), and a methanol solution (20 mL) of potassium hydroxide (16.8 g) was dropwise and gradually added thereto, and heated under reflux for 2 hours. After cooled, the formed crystal was collected through filtration and washed with water. This was dried to give TP-5C (63.3 g, 85%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08211598B2uspto-grants-2012_07