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Water → HCID 86712403, 화합물

HRID 2174198
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HRID 2174198 반응식
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([O:12][C:13]1[C:14]([C:19]([CH3:23])([CH3:22])[CH:20]=[O:21])=[N:15][CH:16]=[CH:17][CH:18]=1)=[CH:7]2.[CH3:24][Mg]Cl.O>O1CCCC1>[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([O:12][C:13]1[C:14]([C:19]([CH3:23])([CH3:22])[CH:20]([OH:21])[CH3:24])=[N:15][CH:16]=[CH:17][CH:18]=1)=[CH:7]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 86712402HCID 86712402, 화합물HCID 178418332HCID 178418332, 화합물

생성물 1

HCID 86712403HCID 86712403, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

0.10 g of 2-[3-(8-fluoro-quinolin-3-yloxy)-pyridin-2-yl]-2-methyl-propioaldehyde were dissolved in 3 ml of tetrahydrofuran. 0.2 ml of a 3.0 M tetrahydrofuran solution of methylmagnesium chloride were added thereto followed by stirring for 30 minutes at 0° C. Subsequently, water was added thereto to stop the reaction. The resultant was then extracted with ethyl acetate followed by distilling off the solvent of the organic layer and purifying by silica gel column chromatography to obtain 0.07 g of 3-[3-(8-fluoro-quinolin-3-yloxy)-pyridin-2-yl]-3-methyl-butan-2-ol.

후처리

  1. customthe reaction
  2. extractionThe resultant was then extracted with ethyl acetate
  3. distillationby distilling off the solvent of the organic layer
  4. custompurifying by silica gel column chromatography

출처 및 근거

ORD 기록
ord-5b243470cf02412a861997cd0c809bb6
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09060517B2

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