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Lithium Hydroxide → 3-Chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoic acid

HRID 1629888
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반응식

HRID 1629888 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[N:13]1[CH:17]([CH3:18])[CH2:16][O:15][C:14]1=[O:19])[C:5]([O:7]CC)=[O:6].[OH-].[Li+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[N:13]1[CH:17]([CH3:18])[CH2:16][O:15][C:14]1=[O:19])[C:5]([OH:7])=[O:6]
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참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 67048447Ethyl 3-chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoate

생성물 1

HCID 667314913-Chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

0.90 g (3.17 mmol) ethyl 3-chloro-4-(4-methyl-2-oxo-oxazolidin-3-yl)-benzoate are stirred for 1 hour in 50 ml of methanol with 10 ml 1-molar aqueous lithium hydroxide solution at ambient temperature. The mixture is then evaporated down to 20 ml i. vac., acidified with conc. hydrochloric acid and extracted with ethyl acetate. The combined organic phases are washed with sat. sodium chloride solution, dried over sodium sulphate and evaporated down i. vac. The residue is crystallised from a little diethyl ether and suction filtered.

후처리

  1. customThe mixture is then evaporated down to 20 ml i
  2. extractionextracted with ethyl acetate
  3. washThe combined organic phases are washed with sat. sodium chloride solution
  4. dry with materialdried over sodium sulphate
  5. customevaporated down i
  6. customThe residue is crystallised from a little diethyl ether and suction
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-9f5a481de27b4c05a0e60a9eb47042e7
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08791103B2

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