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Potassium Hydroxide → 2-(3-Methyl-4-nitrophenyl)acetic acid

HRID 494384
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인쇄 미리보기

반응식

HRID 494384 반응식
[OH-].[K+].C([O:5][C:6](=[O:23])[CH:7]([C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[C:15]([CH3:22])[CH:14]=1)C(OCC)=O)C>CO.O>[CH3:22][C:15]1[CH:14]=[C:13]([CH2:7][C:6]([OH:23])=[O:5])[CH:18]=[CH:17][C:16]=1[N+:19]([O-:21])=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 23130308Diethyl 2-(3-methyl-4-nitrophenyl)malonate

생성물 1

HCID 107503542-(3-Methyl-4-nitrophenyl)acetic acid수율 86.5%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

반응 조건

온도
100 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

Potassium hydroxide (0.168 g) was dissolved in 7 mL of methanol and 1 mL of water, and the 2-(3-methyl-4-nitrophenyl)malonic acid diethyl ester (0.250 g) obtained in Example 1-3a) was dissolved in the solution. The solution was stirred at 100° C. for 2 hours and concentrated. The residue was acidified with 2N hydrochloric acid and extracted with ethyl acetate. The extract was washed with saturated brine, dried over sodium sulfate and concentrated to give the title compound (0.143 g) as a yellow solid.

후처리

  1. concentrationconcentrated
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9a047aa2ebac4aeb97dc9bc3efdce700
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07538140B2

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