1-Butanol → 2-(6-Octyloxy-2-naphthyl)-5-butylbenzooxazole

HRID 5284

반응식

HRID 5284 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12]1[O:13][C:14]3[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][CH2:23][CH3:24])=[CH:17][C:15]=3[N:16]=1)[CH:6]=[CH:5]2.[CH2:25](I)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].[OH-].[K+].C(O)CCC>O>[CH2:25]([O:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12]1[O:13][C:14]3[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][CH2:23][CH3:24])=[CH:17][C:15]=3[N:16]=1)[CH:6]=[CH:5]2)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]

참가 물질

6

실험 절차

In a 30ml round-bottom flask, 0.47 g (1.48 m mole) of 2-(6-hydroxy-2-naphthyl)-5-butylbenzooxazole, 0.43 g (1.79 m mole) of octyl iodide, 0.12 g (1.82 m mole) of potassium hydroxide and 5 ml of butanol were placed, followed by refluxing for 310 minutes. The reaction mixture was poured into water, extracted from ethyl acetate to obtain an organic layer. The organic layer was washed with water dried with mirabilite and dried under reduced pressure to obtain a resultant. The resultant was recrystallized from ethylacetate to obtain a crystal. The crystal was filtered, purified by silica gel column chromatography (eluent: toluene) and recrystallized from acetone to obtain 0.36 g of 2-(6-octyloxy-2-naphthyl)-5-butylbenzooxazole (Yield: 56.6%). ##STR190##

후처리

  1. temperatureby refluxing for 310 minutes
  2. extractionextracted from ethyl acetate
  3. customto obtain an organic layer
  4. washThe organic layer was washed with water
  5. dry with materialdried with mirabilite
  6. customdried under reduced pressure
  7. customto obtain a resultant
  8. customThe resultant was recrystallized from ethylacetate
  9. customto obtain a crystal
  10. filtrationThe crystal was filtered
  11. custompurified by silica gel column chromatography (eluent: toluene)
  12. customrecrystallized from acetone

출처 및 근거

ORD 기록
ord-b2461ebc65244f8f8d1cf4f61ec82c12
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05244596

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