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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Pyridine N-Oxide → Ethyl 5-oxopentanoate

HRID 231002
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인쇄 미리보기

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HRID 231002 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7].C(=O)(O)[O-:12].[Na+].[N+]1([O-])C=CC=CC=1>C1(C)C=CC=CC=1>[O:12]=[CH:2][CH2:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7]
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참가 물질

5

반응물 3

HCID 12753Pyridine N-OxideHCID 84580Ethyl 5-bromovalerateHCID 516892Sodium Bicarbonate

생성물 1

HCID 11137279Ethyl 5-oxopentanoate수율 48.7%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Ethyl 5-bromopentanoate (42 g), sodium bicarbonate (34 g) and pyridine N-oxide (38 g) in toluene (250 ml) are heated together under reflux in an atmosphere of nitrogen with vigorous stirring for 9 hours. After cooling, the product is partitioned with water (400 ml). The toluene layer is separated and the aqueous layer is extracted with a further amount of toluene (100 ml). The combined toluene extracts are dried over magnesium sulphate and the toluene removed by fractional distillation. The residue is distilled under vacuum to give ethyl 5-oxopentanoate as a colourless oil (14.1 g), m.s. M+ 144.

후처리

  1. temperatureunder reflux in an atmosphere of nitrogen
  2. temperatureAfter cooling
  3. customthe product is partitioned with water (400 ml)
  4. customThe toluene layer is separated
  5. extractionthe aqueous layer is extracted with a further amount of toluene (100 ml)
  6. dry with materialThe combined toluene extracts are dried over magnesium sulphate
  7. customthe toluene removed by fractional distillation
  8. distillationThe residue is distilled under vacuum

출처 및 근거

ORD 기록
ord-a6783c418acf471d9a51e7869037a386
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04844892

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