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Methanol → [3-(4-Bromo-2-formyl-phenoxy)-phenyl]-acetic acid methyl ester

HRID 885330
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인쇄 미리보기

반응식

HRID 885330 반응식
[Br:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:8]=[C:9]([CH2:13][C:14]([OH:16])=[O:15])[CH:10]=[CH:11][CH:12]=2)=[C:4]([CH:19]=[O:20])[CH:3]=1.S(Cl)(Cl)=O.[CH3:25]O>>[CH3:25][O:15][C:14](=[O:16])[CH2:13][C:9]1[CH:10]=[CH:11][CH:12]=[C:7]([O:6][C:5]2[CH:17]=[CH:18][C:2]([Br:1])=[CH:3][C:4]=2[CH:19]=[O:20])[CH:8]=1
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 58237510[3-(4-Bromo-2-formyl-phenoxy)-phenyl]-acetic acid

생성물 1

HCID 58237467[3-(4-Bromo-2-formyl-phenoxy)-phenyl]-acetic acid methyl ester

반응 조건

온도
65 °C

실험 절차

To [3-(4-bromo-2-formyl-phenoxy)-phenyl]-acetic acid (1 g, 3.0 mmol) in MeOH (10 mL) was added thionyl chloride (0.43 mL, 6.0 mmol), and the reaction was heated to 65° C. for 2 hours, and then at room temperature overnight. The mixture was quenched with 1N aqueous NaOH and extracted three times with EtOAc, and the combined organic layers were washed with H2O, dried, and concentrated. The residue was purified by silica gel chromatography (20-40% EtOAc in hexanes) to give the desired product (0.7 g); as well as the acetal by-product.

후처리

  1. customat room temperature
  2. customovernight
  3. customThe mixture was quenched with 1N aqueous NaOH
  4. extractionextracted three times with EtOAc
  5. washthe combined organic layers were washed with H2O
  6. customdried
  7. concentrationconcentrated
  8. customThe residue was purified by silica gel chromatography (20-40% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-2bbda38a163c4026be11d52578fcfad8
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242145B2

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