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4-Bromophenol → p-Bromophenyl octyl ether

HRID 36817
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인쇄 미리보기

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HRID 36817 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[CH2:9](Br)[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 78084-BromophenolHCID 81401-BromooctaneHCID 11430Potassium Carbonate

생성물 1

HCID 145298p-Bromophenyl octyl ether수율 63.9%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

In 100 ml of acetone, 8.0 g of 4-bromophenol, 8.9 g of n-octylbromide, and 13 g of potassium carbonate were heated to reflux for 12 hours. After the solvent was distilled off under a reduced pressure, the residue thus obtained was extracted with isopropyl ether, washed with a 5% aqueous sodium hydroxide solution and water in turn. The ether was distilled off, and the residue was purified by a silica gel column chromatography using a mixed solvents of n-hexane and diethyl ether (10:1) and subjected to distillation to obtain 8.4 g of 4-bromo-1-n-octyloxybenzene.

후처리

  1. temperatureto reflux for 12 hours
  2. distillationAfter the solvent was distilled off under a reduced pressure
  3. customthe residue thus obtained
  4. extractionwas extracted with isopropyl ether
  5. washwashed with a 5% aqueous sodium hydroxide solution and water in turn
  6. distillationThe ether was distilled off
  7. customthe residue was purified by a silica gel column chromatography
  8. distillationsubjected to distillation

출처 및 근거

ORD 기록
ord-1008d93569fe4f328b166d92dc104611
출처 데이터셋
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05417885

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