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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tetrahydrofuran → (4-Pyridin-2-YL-phenyl)-acetic acid

HRID 1362784
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반응식

HRID 1362784 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([O:16]C)=[O:15])=[CH:9][CH:8]=1.O1CCCC1.[OH-].[K+]>O>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([OH:16])=[O:15])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 14797Potassium HydroxideHCID 12094242Methyl 2-(4-(pyridin-2-yl)phenyl)acetate

생성물 1

HCID 504301(4-Pyridin-2-YL-phenyl)-acetic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

700 mg (3.11 mol) of methyl [4-(2-pyridyl)phenyl]acetate are introduced into 5 ml of tetrahydrofuran and, at room temperature, 6.2 ml of a 1M potassium hydroxide solution in water are added. The mixture is stirred at room temperature for 18 h and then the solvent is substantially removed in vacuo, the residue is taken up in 10 ml of water and the pH was adjusted to about 5 with 2N hydrochloric acid. Extraction of the aqueous phase twice with 10 ml of dichloromethane each time affords, after drying the combined organic phases over magnesiumsulfate and removing the solvent in vacuo, the compound of Example VIII in the form of a solid.

후처리

  1. customthe solvent is substantially removed in vacuo
  2. extractionExtraction of the aqueous phase twice with 10 ml of dichloromethane each time
  3. customaffords
  4. dry with materialafter drying the combined organic phases over magnesiumsulfate
  5. customremoving the solvent in vacuo

출처 및 근거

ORD 기록
ord-f304a59ac13b458e9d7ba4b592e74e36
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07883713B2

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