تفاعل #1596974

ord-bbbff25e811c444388c682c4814b6bad

معادلة التفاعل

CCOC(=O)c1ccc(O)cc1
Ethyl p-hydroxybenzoate
C=COCCCCCBr
5-bromopentylvinyl ether
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)N(C)C
N,N-dimethylacetamide
C=COCCCCCOc1ccc(C(=O)O)cc1
4-(5-vinyloxypentyloxy)benzoic acid
المردود 128.6%

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
    workup.DISSOLUTIONdissolved in water (1 L)
  14. 14
    workup.ADDITIONConcentrated hydrochloric acid (25.7 mL) was added
  15. 15
    ترشيحthe precipitated crystal was collected through filtration under reduced pressure
  16. 16
    غسيلwashed with water
  17. 17
    أخرىThis was dried

الإجراء التجريبي

Ethyl p-hydroxybenzoate (33.2 g), 5-bromopentylvinyl ether (58.0 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 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 dissolved in water (1 L). Concentrated hydrochloric acid (25.7 mL) was added thereto, and the precipitated crystal was collected through filtration under reduced pressure, and washed with water. This was dried to give 4-(5-vinyloxypentyloxy)benzoic acid (TP-29C) (64.3 g, 90%). Production of 2,3,6,7,10,11-hexa(4-(5-vinyloxypentyloxy)benzoyloxy)triphenylene (TP-29):

المصدر

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