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Hydrochloric Acid → 3-(Furan-2-yl)-2-oxopropanoic acid

HRID 1184320
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인쇄 미리보기

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HRID 1184320 반응식
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7](=[O:11])[C:8]([O-:10])=[O:9].[OH-].[Na+].Cl>>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7](=[O:11])[C:8]([OH:10])=[O:9]
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참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 20497773-(Furan-2-yl)-2-oxopropanoate

생성물 1

HCID 20497783-(Furan-2-yl)-2-oxopropanoic acid수율 57.1%

반응 조건

온도
90 °C

실험 절차

To a 100 mL flask, 3-(furan-2-yl)-2-oxopropanoate (940 mg) along with 23 mL cold 6N NaOH was added. The insoluble mixture was stirred in a 90° C. bath for 5 min until dissolved. Cold 1N HCl was added until solution was acidic (approx 120 mL). Solution was extracted 2×50 mL EtOAc. Combined organic layers were washed with 40 mL brine and dried with Na2SO4. Solution was evaporated to yield 540 mg brown solid. Solid was further purified by reversed-phase high-performance liquid chromatography (HPLC) ramping from 97% aqueous trifluoroacetic acid (TFA) to acetonitrile (ACN).

후처리

  1. dissolutionuntil dissolved
  2. extractionSolution was extracted 2×50 mL EtOAc
  3. washCombined organic layers were washed with 40 mL brine
  4. dry with materialdried with Na2SO4
  5. customSolution was evaporated

출처 및 근거

ORD 기록
ord-58402d3bd7054c958ef2a273569df5de
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08669103B2

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