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Dimethylamine → 3-(4-Chloro-2-nitro-phenoxy)-N,N-dimethyl-benzamide

HRID 2197906
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인쇄 미리보기

반응식

HRID 2197906 반응식
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][CH:15]=2)[C:10](Cl)=[O:11])=[C:4]([N+:18]([O-:20])=[O:19])[CH:3]=1.[CH3:21][NH:22][CH3:23].O>C1COCC1>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][CH:15]=2)[C:10]([N:22]([CH3:23])[CH3:21])=[O:11])=[C:4]([N+:18]([O-:20])=[O:19])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 674DimethylamineHCID 962WaterHCID 866155003-(4-Chloro-2-nitro-phenoxy)-benzoyl chloride

생성물 1

HCID 684583013-(4-Chloro-2-nitro-phenoxy)-N,N-dimethyl-benzamide수율 92.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To the product from Example 168b (2.0 g, 6.4 mmol) in THF (25 mL) was added dimethylamine (0.6 g, 13.3 mmol) and the reaction stirred for 16 h. The reaction was poured into water and extracted with ethyl acetate. The organic layer washed with 5% HCL, water, brine, and dried over sodium sulfate, filtered and concentrated under vacuum giving the title compound (1.9 g, 87%).

후처리

  1. extractionextracted with ethyl acetate
  2. washThe organic layer washed with 5% HCL, water, brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-14b8e40f0be04bcb8d31812498fa0610
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338605B2

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