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Ethylene Glycol → HCID 23130637, 화합물

HRID 2080018
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HRID 2080018 반응식
[N+:1]([C:4]1[S:5][CH:6]=[CH:7][C:8]=1[CH:9]=[O:10])([O-:3])=[O:2].[CH2:11](O)[CH2:12][OH:13].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[N+:1]([C:4]1[S:5][CH:6]=[CH:7][C:8]=1[CH:9]1[O:13][CH2:12][CH2:11][O:10]1)([O-:3])=[O:2]
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참가 물질

6

반응물 4

HCID 174Ethylene GlycolHCID 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrateHCID 105588712-Nitro-3-thiophenecarboxaldehyde

생성물 1

HCID 23130637HCID 23130637, 화합물수율 65%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

2-Nitro-thiophene-3-carbaldehyde described in Preparation Example T-2 (367 mg, 2.33 mmol), ethane-1,2-diol (651 μl, 11.7 mmol) and toluene-4-sulfonic acid monohydrate (40 mg, 0.233 mmol) were dissolved in toluene (8 mL), and the solution was stirred for 2.5 hours under reflux. An aqueous solution of saturated sodium bicarbonate was added to the reaction solution at 0° C., which was then extracted with ethyl acetate, the organic layer was washed with brine, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, the residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=5:1), and the title compound (304 mg, 1.51 mmol, 65%) was obtained as a white solid.

후처리

  1. temperatureunder reflux
  2. extractionwhich was then extracted with ethyl acetate
  3. washthe organic layer was washed with brine
  4. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated in vacuo
  6. customthe residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=5:1)

출처 및 근거

ORD 기록
ord-459482f4b6da4c1c95a597746177a150
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932272B2

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