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1,4-Dioxane → 4,5-Dichloro-2-formylbenzoic acid

HRID 1432370
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HRID 1432370 반응식
Br[CH:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:12])=[C:8]([Cl:11])[CH:9]=2)[C:4](=[O:13])[O:3]1.[O:14]1CCOCC1>Cl>[Cl:11][C:8]1[C:7]([Cl:12])=[CH:6][C:5]([C:4]([OH:3])=[O:13])=[C:10]([CH:2]=[O:14])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 312751,4-DioxaneHCID 144180783-Bromo-5,6-dichloro-3H-isobenzofuran-1-one

생성물 1

HCID 865917864,5-Dichloro-2-formylbenzoic acid수율 73%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A suspension of 3-bromo-5,6-dichloro-3H-isobenzofuran-1-one (2.0 g) in 5% aqueous HCl (10 mL) and 80% aqueous dioxane (25 mL) were heated to reflux for 2 hours. The solvent was removed and the resulting residue re-dissolved in ethyl acetate, dried (magnesium sulfate) and concentrated. The resultant yellow solid was recrystallized from DCM/hexane to give the sub-title compound as a white solid (1.13 g, 73%); 1H NMR (400 MHz, CDCl3) δ 6.66 (0.84H, s), 7.95 (0.16H, s), 8.05 (0.84H), 8.12 (0.16H, s), 8.14 (0.84H, s), 8.41 (0.84H,), 10.41 (0.16H, s), 11.07 (0.16H, brs).

후처리

  1. temperaturewere heated
  2. temperatureto reflux for 2 hours
  3. customThe solvent was removed
  4. dissolutionthe resulting residue re-dissolved in ethyl acetate
  5. dry with materialdried (magnesium sulfate)
  6. concentrationconcentrated
  7. customThe resultant yellow solid was recrystallized from DCM/hexane

출처 및 근거

ORD 기록
ord-4f5767526a7d417ba48aee3cee19de6b
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07612091B2

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