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Ethylene carbonate → 5-Ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-benzaldehyde

HRID 1266699
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HRID 1266699 반응식
[CH2:1]([O:3][C:4]1[C:5]([OH:13])=[CH:6][C:7]([F:12])=[C:8]([CH:11]=1)[CH:9]=[O:10])[CH3:2].C1(=O)O[CH2:17][CH2:16][O:15]1>C1(C)C=CC=CC=1.[I-].C([N+](CCCC)(CCCC)CCCC)CCC>[CH2:1]([O:3][C:4]1[C:5]([O:13][CH2:17][CH2:16][OH:15])=[CH:6][C:7]([F:12])=[C:8]([CH:11]=1)[CH:9]=[O:10])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7303Ethylene carbonateHCID 226475845-Ethoxy-2-fluoro-4-hydroxy-benzaldehyde

생성물 1

HCID 219055785-Ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-benzaldehyde수율 90.8%

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide촉매HCID 1140Toluene용매

실험 절차

The 5-ethoxy-2-fluoro-4-hydroxy-benzaldehyde (9.15 g) described in example 1.3 was dissolved in toluene (80 ml). Ethylene carbonate (5.25 g) and tetrabutylammonium iodide (1.83 g) were added and the mixture was heated to reflux for 22 h. The mixture was cooled to room temperature and filtered over a plug of silica gel. The product was eluted with hexane/ethyl acetate. The solvent was evaporated and the solid was washed with hot hexane to give 10.3 g of 5-ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-benzaldehyde as a slightly orange solid. MS: 228 ([M]+).

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 22 h
  3. filtrationfiltered over a plug of silica gel
  4. washThe product was eluted with hexane/ethyl acetate
  5. customThe solvent was evaporated
  6. washthe solid was washed with hot hexane

출처 및 근거

ORD 기록
ord-f731d73c87cb4ed4aedeea270298d89c
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06548694B2

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