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Methyl 4-{[2-oxodihydro-3(2H)-furanylidene]methyl}benzoate → Methyl 4-[(2-oxotetrahydro-3-furanyl)methyl]benzoate

HRID 2243287
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인쇄 미리보기

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HRID 2243287 반응식
[O:1]=[C:2]1[C:6](=[CH:7][C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)[CH2:5][CH2:4][O:3]1>C(O)(=O)C.[C].[Pd]>[O:1]=[C:2]1[CH:6]([CH2:7][C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)[CH2:5][CH2:4][O:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68707654Methyl 4-{[2-oxodihydro-3(2H)-furanylidene]methyl}benzoate

생성물 1

HCID 21605851Methyl 4-[(2-oxotetrahydro-3-furanyl)methyl]benzoate

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 176Acetic Acid용매

실험 절차

20.00 g (0.09 mol) of methyl 4-([2-oxodihydro-3(2H)-furanylidene]methyl)benzoate from Ex. V are suspended in 240 ml of glacial acetic acid, 2.00 g of 10% palladium-carbon are added and the mixture is hydrogenated at atmospheric pressure for 4 hours. The reaction mixture is filtered through kieselguhr and the solvent is distilled off under reduced pressure.

후처리

  1. filtrationThe reaction mixture is filtered through kieselguhr
  2. distillationthe solvent is distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-bbf21f5454fb4214ba1a55996ba0b37b
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07674825B2

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