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2-Bromophenol → 1-Bromo-2-(2,2-diethoxyethoxy)benzene

HRID 2355395
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HRID 2355395 반응식
[OH-].[K+].[Br:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10].[CH2:11]([O:13][CH:14]([O:17][CH2:18][CH3:19])[CH2:15]Br)[CH3:12]>O.CS(C)=O.CCOCC>[CH2:11]([O:13][CH:14]([O:17][CH2:18][CH3:19])[CH2:15][O:10][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[Br:3])[CH3:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 72442-BromophenolHCID 14797Potassium HydroxideHCID 74852Ethane, 2-bromo-1,1-diethoxy-

생성물 1

HCID 229514321-Bromo-2-(2,2-diethoxyethoxy)benzene

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 3283
Diethyl Ether
용매

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온도
100 °C

실험 절차

A solution of KOH pellets (85%, 0.68 g, 10.3 mmol) in water (1.5 mL) was added to 2-bromophenol (1 mL, 8.6 mmol). The mixture was diluted with DMSO (20 mL) and bromoacetaldehyde diethyl acetal (1.43 mL, 9.5 mmol) was added. The mixture was heated at 100° C. for 6 h, cooled to rt, diluted with ether (175 mL), washed with water (3×40 mL) and 5% aq NaOH (40 mL), and dried over MgSO4. Removal of the solvent left 1-(2,2-diethoxyethoxy)-2-bromobenzene (2.62 g, quant) as an oil.

후처리

  1. additionwas added
  2. temperaturecooled to rt
  3. washwashed with water (3×40 mL) and 5% aq NaOH (40 mL)
  4. dry with materialdried over MgSO4
  5. customRemoval of the solvent
  6. waitleft 1-(2,2-diethoxyethoxy)-2-bromobenzene (2.62 g, quant) as an oil

출처 및 근거

ORD 기록
ord-2413596cbc1b4467bf4a6cb999c51643
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754737B2

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