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Sodium Hydroxide → 2-(2-Chloro-4-nitrophenyl)acetic acid

HRID 1454693
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HRID 1454693 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH:11](C(OCC)=O)[C:12]([O:14]CC)=[O:13].[OH-].[Na+]>CO>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH2:11][C:12]([OH:14])=[O:13]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 21875913Diethyl 2-(2-chloro-4-nitrophenyl)malonate

생성물 1

HCID 125105882-(2-Chloro-4-nitrophenyl)acetic acid수율 87%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
50 °C

실험 절차

To a solution of diethyl 2-(2-chloro-4-nitrophenyl)malonate (step 1, 7.6 g, 24.2 mmol) in methanol (18 ml) was added 6M-NaOH (12 ml) and stirred for 1 h at 50° C. The reaction was quenched by the addition of saturated citric acid aqueous solution (16 ml) and water. The organic layer was extracted with ethyl acetate (2×50 ml), washed with brine, dried (MgSO4) and concentrated to give 4.52 g (87%) of title compound as light yellow solid.

후처리

  1. customThe reaction was quenched by the addition of saturated citric acid aqueous solution (16 ml) and water
  2. extractionThe organic layer was extracted with ethyl acetate (2×50 ml)
  3. washwashed with brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-44fdfd97d3634a0ca0c7a2ba4e918246
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07479564B2

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