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Sodium Hydroxide → (3-Methoxy-4-nitrophenyl)acetic acid

HRID 1503845
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HRID 1503845 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:12](C(OCC)=O)[C:13]([O:15]CC)=[O:14])[CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10].[OH-].[Na+]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:12][C:13]([OH:15])=[O:14])[CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 70559053HCID 70559053, 화합물

생성물 1

HCID 16755859(3-Methoxy-4-nitrophenyl)acetic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of the product of EXAMPLE 30A (0.3 g, 0.96 mmol) in ethanol (2 mL) was added 2N aqueous sodium hydroxide (2 mL) and the mixture was stirred at room temperature for 12 hours. Ater concentration, the residue was diluted with water and extracted with ethyl acetate. The aqueous phase was acidified to pH 2-3 with concentrated HCl and extracted with ethyl acetate (3×5 mL). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The title compound was used in the next step without further purification.

후처리

  1. concentrationAter concentration
  2. additionthe residue was diluted with water
  3. extractionextracted with ethyl acetate
  4. extractionextracted with ethyl acetate (3×5 mL)
  5. washThe combined organic phase was washed with brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe title compound was used in the next step without further purification

출처 및 근거

ORD 기록
ord-f248bbfd396748dbbdabee65ecda519f
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09212192B2

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