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Acetic Acid → HCID 11823172, 화합물

HRID 1938573
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HRID 1938573 반응식
[CH3:1][Si:2]([CH3:12])([CH3:11])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH2:6][OH:7].C1C=CC(N=NC2C=CC(N)=NC=2N)=CC=1.Cl.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.C(O)(=O)C>ClCCl>[CH3:1][Si:2]([CH3:12])([CH3:11])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 151146973-(Trimethylsilyl)benzenemethanolHCID 86587493Pyridium dichromate

생성물 1

HCID 11823172HCID 11823172, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a mixture of 3-trimethylsilylbenzylalcohol (3.60 g, 20 mmol) and pyridium dichromate (11.29 g, 30 mmol) in dichloromethane (60 ml) at 0° C. was added 3 Å molecular sieve powder (16 g) and anhydrous acetic acid (2 ml). Then the reaction was allowed to react 30 min at room temperature, stirred 20 min with celite (10 g), filtered and evaporated under reduced pressure. The residue was treated with diethyl ether (50 ml), filtered through MgSO4 and concentrated. 3-trimethylsilylbenzaldehyde was purified by distillation.

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후처리

  1. customto react 30 min at room temperature
  2. filtrationfiltered
  3. customevaporated under reduced pressure
  4. additionThe residue was treated with diethyl ether (50 ml)
  5. filtrationfiltered through MgSO4
  6. concentrationconcentrated
  7. distillation3-trimethylsilylbenzaldehyde was purified by distillation

출처 및 근거

ORD 기록
ord-7bc48bb658064b1c92353d48a6a9c711
출처 데이터셋
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05693668

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