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Ethylene Glycol → 3-(1,3-Dioxolan-2-yl)-6-methoxybenzofuran

HRID 273338
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인쇄 미리보기

반응식

HRID 273338 반응식
[CH3:1][O:2][C:3]1[CH:13]=[CH:12][C:6]2[C:7]([CH:10]=[O:11])=[CH:8][O:9][C:5]=2[CH:4]=1.[OH:14][CH2:15][CH2:16]O.O>C1C=CC=CC=1>[O:11]1[CH2:16][CH2:15][O:14][CH:10]1[C:7]1[C:6]2[CH:12]=[CH:13][C:3]([O:2][CH3:1])=[CH:4][C:5]=2[O:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 962WaterHCID 824109866-Methoxybenzofuran-3-carbaldehyde

생성물 1

HCID 691945443-(1,3-Dioxolan-2-yl)-6-methoxybenzofuran수율 95%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A mixture of 6-methoxybenzofuran-3-carbaldehyde (0.600 g, 3.41 mmol), HOCH2CH2OH (3.17 g, 51 mmol) and p-toluenesulfonic acids (0.001 g) in benzene (20 mL) was refluxed for 8 h using a Dean-Stark water trap. The mixture was concentrated under reduced pressure and then diluted with EtOAc. The organic solution was washed with water, dried over anhydrous MgSO4, and concentrated to give 3-(1,3-dioxolan-2-yl)-6-methoxybenzofuran (0.711 g, 95%)

후처리

  1. temperaturewas refluxed for 8 h
  2. concentrationThe mixture was concentrated under reduced pressure
  3. additiondiluted with EtOAc
  4. washThe organic solution was washed with water
  5. dry with materialdried over anhydrous MgSO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b85f95c64a904ebdba1cf6a4ca14aca7
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07456289B2

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