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Water → 2-(3-Cyano-4-fluorophenyl)acetic acid

HRID 2173228
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HRID 2173228 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:7]([CH2:10][CH:11]=C)=[CH:6][C:3]=1[C:4]#[N:5].I([O-])(=O)(=O)=[O:14].[Na+].[OH2:19]>C(Cl)(Cl)(Cl)Cl.C(#N)C.C(Cl)Cl.O.[Ru]=O>[C:4]([C:3]1[CH:6]=[C:7]([CH2:10][C:11]([OH:14])=[O:19])[CH:8]=[CH:9][C:2]=1[F:1])#[N:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 3

HCID 962Water2회HCID 23667635Sodium periodateHCID 247217703-(3-Cyano-4-fluorophenyl)-1-propene

생성물 1

HCID 27739352-(3-Cyano-4-fluorophenyl)acetic acid

시약·촉매·용매 4

HCID 178526987HCID 178526987, 화합물촉매HCID 5943Carbon Tetrachloride용매
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 6342
Acetonitrile
용매
HCID 6344Dichloromethane용매

실험 절차

A stirred solution of 2-fluoro-5-(prop-2-en-1-yl)benzonitrile (1.9 g, 11.8 mmol) in CCl4 (25 mL), acetonitrile (25 mL) and water (38 mL) was added sodium periodate (8.83 g, 41.3 mmol) and ruthenium oxide hydrate (200 mg) and the resulting mixture was stirred at ambient temperature overnight. The mixture was diluted with 100 mL DCM and 100 mL of water. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified with silica gel column chromatography afford crude (3-cyano-4-fluorophenyl)acetic acid.

후처리

  1. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  2. concentrationconcentrated
  3. customThe residue was purified with silica gel column chromatography

출처 및 근거

ORD 기록
ord-03de31c9935f4d4a9f35e42bcd69b928
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09056859B2

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