1-Bromohexane → 2,6-Dibromo-1,5-bis(hexyloxy)naphthalene

HRID 645306노트

반응식

HRID 645306 반응식
[O-][CH2:2][CH3:3].[Na+].[Br:5][C:6]1[CH:15]=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([Br:17])[C:12]=2[OH:16])[C:7]=1[OH:18].[CH2:19](Br)[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]>C(O)C>[Br:5][C:6]1[CH:15]=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([Br:17])[C:12]=2[O:16][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:7]=1[O:18][CH2:15][CH2:6][CH2:7][CH2:8][CH2:2][CH3:3]

참가 물질

5

반응물 3

HCID 81011-BromohexaneHCID 962602,6-Dibromo-1,5-naphthalenediolHCID 2723922Sodium ethoxide

생성물 1

HCID 183321032,6-Dibromo-1,5-bis(hexyloxy)naphthalene수율 48%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

Under an inert atmosphere, sodium ethoxide (2.76 g, 40.6 mmol) and 2,6-dibromo-1,5-di hydroxynaphthalene (5 g, 15.7 mmol) were dissolved in ethanol (60 ml). Under reflux, ethanol solution (10 ml) of hexylbromide (6.7 g, 40.6 mmol) was added dropwise in 10 minutes. It was refluxed for 5 hours and then left for cooling. The reaction mixture was added to 1N sodium-hydroxide aqueous solution, and the depositing precipitate was filtrated. The precipitate was washed with methylene chloride, and the washed solution was concentrated under a reduced pressure to obtain a crude product. The desired product was obtained after purifying by silica gel chromatography (toluene:hexane=4:1).

후처리

  1. temperatureUnder reflux
  2. temperatureIt was refluxed for 5 hours
  3. waitleft
  4. temperaturefor cooling
  5. additionThe reaction mixture was added to 1N sodium-hydroxide aqueous solution
  6. filtrationthe depositing precipitate was filtrated
  7. washThe precipitate was washed with methylene chloride
  8. concentrationthe washed solution was concentrated under a reduced pressure
  9. customto obtain a crude product

출처 및 근거

ORD 기록
ord-1fec327efe3a452790a109fd95f209c2
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07701129B2

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