تفاعل #1596974
ord-bbbff25e811c444388c682c4814b6bad
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةAfter cooled
- 2استخلاصextracted with ethyl acetate (500 mL)
- 3غسيلwashed two times with water (100 mL)
- 4تجفيفThis was dried with anhydrous magnesium sulfate
- 5ترشيحfiltered
- 6أخرىThe solvent was removed through concentration under reduced pressure
- 7workup.DISSOLUTIONthe residue was dissolved in methanol (100 mL)
- 8workup.ADDITIONgradually added
- 9درجة الحرارةheated
- 10درجة الحرارةunder reflux for 2 hours
- 11درجة الحرارةAfter cooled
- 12ترشيحthe formed crystal was collected through filtration
- 13workup.DISSOLUTIONdissolved in water (1 L)
- 14workup.ADDITIONConcentrated hydrochloric acid (25.7 mL) was added
- 15ترشيحthe precipitated crystal was collected through filtration under reduced pressure
- 16غسيلwashed with water
- 17أخرىThis 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):