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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromine → Ethyl 2-bromo-4-methyl-3-oxopentanoate

HRID 241681
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인쇄 미리보기

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HRID 241681 반응식
C([O-])(=O)C.[Na+].[CH2:6]([O:8][C:9](=[O:16])[CH2:10][C:11](=[O:15])[CH:12]([CH3:14])[CH3:13])[CH3:7].[Br:17]Br>C(O)(=O)C>[Br:17][CH:10]([C:11](=[O:15])[CH:12]([CH3:13])[CH3:14])[C:9]([O:8][CH2:6][CH3:7])=[O:16]
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참가 물질

5

반응물 3

HCID 24408BromineHCID 81583Ethyl isobutyrylacetateHCID 517045Sodium Acetate

생성물 1

HCID 13015595Ethyl 2-bromo-4-methyl-3-oxopentanoate

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
10 °C

실험 절차

To a suspension of sodium acetate (1.9 g) in glacial acetic acid (15 ml) was added 4-methyl-3-oxo-pentanoic acid ethyl ester (2 g) and the reaction mixture cooled to 10° C. Bromine (0.7 ml) was then added dropwise. The resulting solution was allowed to warm to room temperature and stirred for 1 h. The reaction was complete (by TLC) and was concentrated in vacuum affording 3.8 g crude ethyl product which was used directly in the next synthetic step.

후처리

  1. temperatureto warm to room temperature
  2. concentrationwas concentrated in vacuum
  3. customaffording 3.8 g crude ethyl product which

출처 및 근거

ORD 기록
ord-99684f208e914c6eb1a480b128c8d64c
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653075B2

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