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3-Hydroxyacetanilide → HCID 22722095, 화합물

HRID 1581681
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HRID 1581681 반응식
I[C:2]1[CH:11]=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:12]([NH:15][C:16]1[CH:17]=[C:18]([OH:22])[CH:19]=[CH:20][CH:21]=1)(=[O:14])[CH3:13]>CC(N(C)C)=O.[Cu-]=O>[C:12]([NH:15][C:16]1[CH:17]=[C:18]([CH:19]=[CH:20][CH:21]=1)[O:22][C:2]1[CH:11]=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5])(=[O:14])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 121243-HydroxyacetanilideHCID 69132Benzoic acid, 2-iodo-, methyl ester

생성물 1

HCID 22722095HCID 22722095, 화합물수율 55%

시약·촉매·용매 2

HCID 178419072HCID 178419072, 화합물촉매HCID 31374Dimethylacetamide용매

반응 조건

온도
180 °C

실험 절차

To a stirred solution of methyl 2-iodobenzoate (10 g, 38.2 mmole) in dimethylacetamide (50 mL) was added 3-acetamidophenol (5 g, 33 mmole) and copper(I) oxide (2.5 g, 17 mmole), and the mixture was heated at reflux under argon (180° C. oil bath). After 24 h the reaction was cooled to RT and most of the solvent was distilled off. The remaining residue was purified by flash chromatography on silica gel (50% EtOAc/hexane) to give the crude title compound (4.95, 55%): MS (ES) m/e 286.2 (M+H)+. The title compound prepared in this way contained approximately 45% N,O-diarylated acetamidophenol as a contaminant: MS (ES) m/e 420.4 (M+H)+. The mixture was used without further purification.

후처리

  1. temperaturethe mixture was heated
  2. temperatureAfter 24 h the reaction was cooled to RT and most of the solvent
  3. distillationwas distilled off
  4. customThe remaining residue was purified by flash chromatography on silica gel (50% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-1b1f33a9762048d4b8bf2650c870abff
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06730684B1

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