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Triethylamine → Acetaldehyde, 2-(2-phenylethoxy)-

HRID 863846
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HRID 863846 반응식
[C:1]1([CH2:7][CH2:8][O:9][CH2:10][CH2:11][OH:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CCN(CC)CC>CS(C)=O.C(Cl)Cl.CCOCC>[C:1]1([CH2:7][CH2:8][O:9][CH2:10][CH:11]=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

5

반응물 2

HCID 8471TriethylamineHCID 132089292-(2-Phenylethoxy)ethanol

생성물 1

HCID 162493Acetaldehyde, 2-(2-phenylethoxy)-

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 21912085Dimethylsulfoxide-dichloromethane용매

실험 절차

To 2-(2-phenylethoxy)-1-ethanol (0.25 g; 1.5 mmol) [J. Med. Chem., 1570 (1983)] dissolved in DMSO/CH2Cl2 (4 ml/2 ml) is added Et3N (1 ml; 7 mmol) followed by sulfur trioxide pyridine complex (1.2 g; 7.5 mmol). After 10 minutes, the reaction mixture is then diluted with Et2O and washed with brine, 1N HCl, NaHCO3 and brine, dried (MgSO4) and concentrated in vacuo to dryness. The residue is purified by column chromatography using CH2Cl2 to obtain 2-phenylethoxyacetaldehyde which is used directly in Step B.

후처리

  1. washwashed with brine, 1N HCl, NaHCO3 and brine
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated in vacuo to dryness
  4. customThe residue is purified by column chromatography

출처 및 근거

ORD 기록
ord-275b6da7e74f405585cb46aea7d935ec
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05561143

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