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Dimethylformamide → 1-Bromo-5-isopropyl-2,4-bis-methoxymethoxy-benzene

HRID 1947173
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HRID 1947173 반응식
[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[C:5]([OH:11])=[CH:4][C:3]=1[OH:12].CN(C)[CH:15]=[O:16].[CH2:18](N(C(C)C)C(C)C)C.[CH3:27][O:28][CH2:29]Cl>C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[C:5]([O:11][CH2:27][O:28][CH3:29])=[CH:4][C:3]=1[O:12][CH2:18][O:16][CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 7864Chloromethyl Methyl EtherHCID 81531DiisopropylethylamineHCID 598299224-Bromo-6-(propan-2-YL)benzene-1,3-diol

생성물 1

HCID 598298701-Bromo-5-isopropyl-2,4-bis-methoxymethoxy-benzene수율 83.1%

시약·촉매·용매 1

HCID 8857
Ethyl Acetate
용매

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온도
0 °C

실험 절차

4-bromo-6-isopropyl-benzene-1,3-diol (IM1-a: 10.5 g, 45.5 mmol), dimethyl formamide (50 mL) and ethyldiisopropylamine (39.6 mL, 227 mmol) were placed in a 100 mL eggplant shaped flask, and the solution was cooled to 0° C., mixed with methoxymethylchloride (17.3 mL, 227 mmol) and the mixture was allowed to come to room temperature. After stirring for 12 hours the solution was heated to 50° C. and stirring was continued further for 6.5 hours. After completing the reaction, ethyl acetate was added, and after washing the organic layer 4 times with saturated sodium chloride, the organic layer was dried anhydrous sodium sulfate. After filtration and evaporation, the residue was purified by silica gel column chromatography to obtain the title compound (IM2-a: 12.1 g, 83.1%).

후처리

  1. customto come to room temperature
  2. temperaturewas heated to 50° C.
  3. stirringstirring
  4. waitwas continued further for 6.5 hours
  5. additionwas added
  6. washafter washing the organic layer 4 times with saturated sodium chloride
  7. filtrationAfter filtration and evaporation
  8. customthe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-0feda5b19cb3441c9966e115d8d35797
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399464B2

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