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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Toluene → Ethyl 2-(1-methyl-2-oxocyclopentyl)acetate

HRID 1438921
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HRID 1438921 반응식
C1(C)C=CC=CC=1.[CH3:8][CH:9]1[CH2:13][CH2:12][CH2:11][C:10]1=[O:14].Br[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18]>C1C=CC=CC=1>[CH2:20]([O:19][C:17](=[O:18])[CH2:16][C:9]1([CH3:8])[CH2:13][CH2:12][CH2:11][C:10]1=[O:14])[CH3:21]
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 7748Ethyl bromoacetateHCID 142652-Methylcyclopentanone

생성물 1

HCID 12292030Ethyl 2-(1-methyl-2-oxocyclopentyl)acetate

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A solution of sodium tert.-amylate in toluene (70 ml, 0.1 mole) is added dropwise with stirring under an atmosphere of nitrogen to a solution of 2-methylcyclopentanone (9.8 g, 0.1 mole) and ethyl bromoacetate (16.7 g, 0.1 mole) in dry benzene (100 ml). The reaction is exothermic, a precipitate is formed, and the mixture turns yellow-orange. Stirring is continued for 3 hrs. at room temperature, the solution is washed with 1% HCl, cold water, and brine, dried over anhydrous magnesium sulfate and the solvent evaporated to yield 1-methyl-2-oxocyclopentane acetic acid ethyl ester as a pale yellow oil which is used without further purification in the subsequent step and which is identical with the same compound described in Example 5.

후처리

  1. customa precipitate is formed
  2. washat room temperature, the solution is washed with 1% HCl, cold water, and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-7a342331d404476e8fb65aada73f77cf
출처 데이터셋
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04057559

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