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Water → HCID 57630055, 화합물

HRID 600976
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HRID 600976 반응식
C([O:3][C:4](=[O:23])/[C:5](=[N:16]/[O:17][CH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1)/[C:6]1[CH:11]=[CH:10][C:9]([S:12]([CH3:15])(=[O:14])=[O:13])=[CH:8][CH:7]=1)C.[OH-].[Li+].O>C(O)C>[CH:18]1([O:17]/[N:16]=[C:5](\[C:6]2[CH:7]=[CH:8][C:9]([S:12]([CH3:15])(=[O:14])=[O:13])=[CH:10][CH:11]=2)/[C:4]([OH:23])=[O:3])[CH2:22][CH2:21][CH2:20][CH2:19]1
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참가 물질

5

반응물 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 57631022HCID 57631022, 화합물

생성물 1

HCID 57630055HCID 57630055, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

(E)-Cyclopentyloxyimino-(4-methanesulfonyl-phenyl)-acetic acid ethyl ester (60 mg, 0.18 mmol) was dissolved in ethanol (1.75 mL) and cooled to 0° C. A 2.0 N solution of lithium hydroxide in water (258 μL, 0.52 mmol) was added dropwise and the cooling bath was removed. After stirring 40 min, the reaction mixture was diluted with chloroform (30 mL) and washed with 0.2 M aqueous potassium bisulfate (20 mL). The aqueous phase was extracted with chloroform (30 mL) and the combined organic phases were dried over magnesium sulfate and evaporated in vacuo to afford (E)-cyclopentyloxyimino-(4-methanesulfonyl-phenyl)-acetic acid as a clear, colorless film that was used without further purification.

후처리

  1. customthe cooling bath was removed
  2. additionthe reaction mixture was diluted with chloroform (30 mL)
  3. washwashed with 0.2 M aqueous potassium bisulfate (20 mL)
  4. extractionThe aqueous phase was extracted with chloroform (30 mL)
  5. dry with materialthe combined organic phases were dried over magnesium sulfate
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-4ec5fa15f408463ea148ba7701547c25
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902248B2

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