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Ethylene Glycol → 2-Bromo-4-[1,3]dioxin-2-yl-benzoic acid methyl ester

HRID 2261803
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HRID 2261803 반응식
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[O:11])=[CH:6][C:5]=1[Br:12].[CH2:14]([OH:17])[CH2:15]O.[C:18]1(C)C=CC(S(O)(=O)=O)=CC=1>C1COCC1>[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[O:17][CH2:14][CH:15]=[CH:18][O:11]2)=[CH:6][C:5]=1[Br:12]
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참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 57443308Methyl 2-bromo-4-formylbenzoate

생성물 1

HCID 675288602-Bromo-4-[1,3]dioxin-2-yl-benzoic acid methyl ester수율 729.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The mixture of 2-bromo-4-formyl-benzoic acid methyl ester (440 mg, 1.8 mmol), ethylene glycol (1.1 g, 18 mmol) and p-toluene sulfonic acid (30 mg) in THF (10 mL) is stirred at room temperature overnight. The reaction mixture is partitioned between EtOAc (30 mL) and water (30 mL). The organic phase is washed with brine (30 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography to afford the title compound as syrup (380 mg, 73%). LC-ES/MS m/e 287.0 (M+1).

후처리

  1. customThe reaction mixture is partitioned between EtOAc (30 mL) and water (30 mL)
  2. washThe organic phase is washed with brine (30 mL)
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure to a residue
  6. customThe residue is purified by flash chromatography

출처 및 근거

ORD 기록
ord-3080c20b80154a3d87cf8b0a0f670158
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846960B2

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