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1-Chloro-2-methoxy-4-methylbenzene → 4-Chloro-3-methoxybenzaldehyde

HRID 734749
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반응식

HRID 734749 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][CH3:10].CC(O)=[O:13].O>O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[O:13])=[CH:4][C:3]=1[O:9][CH3:10]
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참가 물질

4

반응물 2

HCID 993521-Chloro-2-methoxy-4-methylbenzeneHCID 21899381Acetic acid--water (1/1)2회

생성물 1

HCID 129097254-Chloro-3-methoxybenzaldehyde수율 89%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Ceric ammonium nitrate (43.3 g, 79.0 mmol, 4.00 equiv) was dissolved in 1:1 HOAc/H2O (200 mL). This solution was added dropwise over one hour to a stirred solution of the product from Step 1 (3.09 g, 19.7 mmol, 1.00 equiv) in 1:1 HOAc/H2O (100 mL) at 100° C. After the addition was complete, the reaction was stirred for an additional 15 minutes. The reaction was cooled, diluted with H2O and extracted twice with Et2O. The combined organic extracts were washed three times with H2O, three times with satd. NaHCO3, and once with brine. The organic phase was dried over MgSO4 and concentrated en vacuo to afford the title compound (3.00 g, 89%) as an amber oil. 1H NMR (400 MHz, CDCL3) 9.97 (s, 1H), 7.57 (d, 1H), 7.46 (s, 1H), 7.43 (d, 1H), 4.00 (s, 3H).

후처리

  1. additionAfter the addition
  2. temperatureThe reaction was cooled
  3. extractionextracted twice with Et2O
  4. washThe combined organic extracts were washed three times with H2O, three times with satd
  5. dry with materialThe organic phase was dried over MgSO4
  6. concentrationconcentrated en vacuo

출처 및 근거

ORD 기록
ord-fa2997c126424bbe8b084fbde9bfe0a7
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592357B2

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