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Methanol → HCID 86705339, 화합물

HRID 587984
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HRID 587984 반응식
[C:1]([O:5][C:6]([C:8]1[S:12][C:11](/[CH:13]=[C:14](\[CH2:18][CH3:19])/[C:15]([OH:17])=[O:16])=[CH:10][CH:9]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CO.C(Cl)(Cl)Cl>C(OCC)(=O)C.[OH-].[Pd+2].[OH-]>[C:1]([O:5][C:6]([C:8]1[S:12][C:11]([CH2:13][CH:14]([CH2:18][CH3:19])[C:15]([OH:17])=[O:16])=[CH:10][CH:9]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 887MethanolHCID 6212ChloroformHCID 90018946HCID 90018946, 화합물

생성물 1

HCID 86705339HCID 86705339, 화합물수율 100.1%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매2회HCID 8857Ethyl Acetate용매

실험 절차

(E)-3-(5-tert-butoxycarbonylthiophen-2-yl)-2-ethylpropenoic acid (20.43 g, 72.4 mmol) was dissolved in ethyl acetate (300 mL), methanol (20 mL) and chloroform (10 mL), palladium hydroxide (2.0 g) was added, and the mixture was stirred at room temperature overnight under a hydrogen atmosphere. After completion of the reaction, palladium hydroxide was removed by celite filtration, and the solvent was evaporated under reduced pressure to give the title compound (20.6 g, quantitative).

후처리

  1. customwas removed by celite filtration
  2. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-fa4122911aa04e8cad7b354c57c3db01
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227949B2

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