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Water → N-methyl-N-[1-(4-nitrophenyl)pyrrolidin-3-yl]acetamide

HRID 1354660
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HRID 1354660 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[CH3:11][N:12]([CH:16]1[CH2:20][CH2:19][NH:18][CH2:17]1)[C:13](=[O:15])[CH3:14].C(=O)([O-])[O-].[Cs+].[Cs+].O>CN(C=O)C>[CH3:11][N:12]([CH:16]1[CH2:20][CH2:19][N:18]([C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=2)[CH2:17]1)[C:13](=[O:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 9590p-FluoronitrobenzeneHCID 10796Cesium carbonateHCID 130411303-(N-Acetyl-N-methylamino)pyrrolidine

생성물 1

HCID 21105631N-methyl-N-[1-(4-nitrophenyl)pyrrolidin-3-yl]acetamide

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4-Fluoronitrobenzene (25.0 g) was slowly added to a suspension of N-methyl-N-pyrrolidin-3-ylacetamide (25.2 g) and cesium carbonate (57.6 g) in DMF (300 ml). After 2 hours, the reaction mixture was poured into water, and the resultant precipitate was filtered off with suction. Alternatively, the product can also be extracted with ethyl acetate and purified by chromatography after concentration. This results in the product with the molecular weight of 263.30 (C13H17N3O3): MS (ESI): 264 (M+H+).

후처리

  1. filtrationthe resultant precipitate was filtered off with suction
  2. extractionAlternatively, the product can also be extracted with ethyl acetate
  3. custompurified by chromatography
  4. concentrationafter concentration
  5. customThis results in the product with the molecular weight of 263.30 (C13H17N3O3)

출처 및 근거

ORD 기록
ord-fcadeb1a2868451aa48fa7d875d05b01
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07223788B2

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