반응 #1596974
ord-bbbff25e811c444388c682c4814b6bad
반응 방정식
용매
반응 조건
후처리
- 1온도After cooled
- 2추출extracted with ethyl acetate (500 mL)
- 3세척washed two times with water (100 mL)
- 4건조This was dried with anhydrous magnesium sulfate
- 5여과filtered
- 6기타The solvent was removed through concentration under reduced pressure
- 7workup.DISSOLUTIONthe residue was dissolved in methanol (100 mL)
- 8workup.ADDITIONgradually added
- 9온도heated
- 10온도under reflux for 2 hours
- 11온도After cooled
- 12여과the formed crystal was collected through filtration
- 13workup.DISSOLUTIONdissolved in water (1 L)
- 14workup.ADDITIONConcentrated hydrochloric acid (25.7 mL) was added
- 15여과the precipitated crystal was collected through filtration under reduced pressure
- 16세척washed with water
- 17기타This was dried
실험 절차
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):