4-Methyl-2-oxovaleric acid → Ethyl 3-bromo-4-methyl-2-oxopentanoate

HRID 244623

반응식

HRID 244623 반응식
[CH3:1][CH:2]([CH3:9])[CH2:3][C:4](=[O:8])[C:5]([OH:7])=[O:6].[CH:10]1[CH:15]=C[NH+]=CC=1.[Br:16][Br-]Br>C(O)(=O)C>[Br:16][CH:3]([CH:2]([CH3:9])[CH3:1])[C:4](=[O:8])[C:5]([O:7][CH2:15][CH3:10])=[O:6]

참가 물질

3

반응 조건

온도
20 °C

실험 절차

To a solution of 4-methyl-2-oxopentanoic acid (5 g) in acetic acid (40 ml) was added pyridine hydrobromide perbromide (12.3 g) and the mixture stirred at 20° C. for 18 hr, then the solvent was removed in vacuo. The residue was dissolved in DCM (100 ml) and washed with water (100 ml), separated by hydrophobic frit and evaporated. The residue was taken up in ethanol (100 ml) and treated with concentrated sulphuric acid (1 ml) and heated at reflux for 18 h, then concentrated in vacuo to approx 30 ml. The mixture was diluted with water (250 ml) and extracted with diethyl ether (100 ml), dried over sodium sulphate and evaporated to give the title compound as a pale yellow oil (5.3 g).

후처리

  1. customthe solvent was removed in vacuo
  2. dissolutionThe residue was dissolved in DCM (100 ml)
  3. washwashed with water (100 ml)
  4. customseparated by hydrophobic frit
  5. customevaporated
  6. additiontreated with concentrated sulphuric acid (1 ml)
  7. temperatureheated
  8. temperatureat reflux for 18 h
  9. concentrationconcentrated in vacuo to approx 30 ml
  10. additionThe mixture was diluted with water (250 ml)
  11. extractionextracted with diethyl ether (100 ml)
  12. dry with materialdried over sodium sulphate
  13. customevaporated

출처 및 근거

ORD 기록
ord-555e5145f1344fa6a5e3a477d46929df
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08658635B2

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