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Diethyl Malonate → Diethyl isopentylmalonate

HRID 373863
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HRID 373863 반응식
[Na].[C:2]([O:10][CH2:11][CH3:12])(=[O:9])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[O-]CC.[Na+:16].[CH2:17](Br)[CH2:18][CH:19]([CH3:21])[CH3:20]>C(O)C>[O-:5][CH2:4][CH3:3].[Na+:16].[CH2:17]([CH:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[C:2]([O:10][CH2:11][CH3:12])=[O:9])[CH2:18][CH:19]([CH3:21])[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 7761Diethyl MalonateHCID 78911-Bromo-3-methylbutaneHCID 2723922Sodium ethoxideHCID 5360545Sodium

생성물 2

HCID 79384Diethyl isopentylmalonateHCID 2723922Sodium ethoxide

시약·촉매·용매 1

HCID 702Ethanol
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용매
2회

실험 절차

Sodium ethoxide was prepared from sodium metal (9.1 g) and freshly distilled absolute ethanol (250 ml). Diethyl malonate (63.5 g) was added to sodium ethoxide in ethanol, and the mixture was stirred at 60°-70° C. for 50 min. Isoamyl bromide (60 g) was added, and the reaction mixture was heated under reflux overnight. After the usual work-up, the resulting crude product was distilled under reduced pressure to give diethyl isoamylmalonate. Yield : 71.7 g (78%).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux overnight
  3. distillationAfter the usual work-up, the resulting crude product was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-4dbddbb96e704ff2a5630d54f6021cf3
출처 데이터셋
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05166174

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