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Diethyl Ether → 4-Bromo-2-fluoro-5-(methoxymethoxy)benzaldehyde

HRID 2236487
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HRID 2236487 반응식
[Br:1][C:2]1[C:9]([OH:10])=[CH:8][C:5]([CH:6]=[O:7])=[C:4]([F:11])[CH:3]=1.[CH2:12](Cl)[O:13][CH3:14].[H-].[Na+].CCOCC>CN(C)C=O>[Br:1][C:2]1[C:9]([O:10][CH2:12][O:13][CH3:14])=[CH:8][C:5]([CH:6]=[O:7])=[C:4]([F:11])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 7864Chloromethyl Methyl EtherHCID 24758Sodium hydrideHCID 59300378HCID 59300378, 화합물

생성물 1

HCID 593002954-Bromo-2-fluoro-5-(methoxymethoxy)benzaldehyde

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
0 °C

실험 절차

4-Bromo-2-fluoro-5-hydroxy-benzaldehyde (750 mg, 3.41 mmol) and MOMCl (545 mg, 6.82 mmol) were dissolved in anhydrous N,N-dimethylformamide (5 mL) and cooled to 0° C. NaH (160 mg, 60% suspension in mineral oil, 4 mmol) is then added. The resulting mixture is allowed to stir at room temperature for 1 h. Ether is then added and washed with H2O (3×20 mL) and brine. After dried over Na2SO4, the ether is removed and the residue is purified through chromatography to afford the desired MOM ether (700 mg, 78%).

후처리

  1. washwashed with H2O (3×20 mL) and brine
  2. dry with materialAfter dried over Na2SO4
  3. customthe ether is removed
  4. customthe residue is purified through chromatography
  5. customto afford the desired MOM ether (700 mg, 78%)

출처 및 근거

ORD 기록
ord-e1922472764e430ba5b08652c2d7bf12
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07713994B2

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