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Methyl iodide → HCID 19980329, 화합물

HRID 1461255
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HRID 1461255 반응식
[H-].[Na+].[C:3]([NH:10][C:11]1[C:16]([CH3:17])=[CH:15][CH:14]=[CH:13][C:12]=1[N+:18]([O-:20])=[O:19])([C:5]([O:7][CH2:8][CH3:9])=[O:6])=[O:4].[CH3:21]I>CN(C=O)C>[C:3]([N:10]([CH3:21])[C:11]1[C:16]([CH3:17])=[CH:15][CH:14]=[CH:13][C:12]=1[N+:18]([O-:20])=[O:19])([C:5]([O:7][CH2:8][CH3:9])=[O:6])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 15525662Acetic acid, [(2-methyl-6-nitrophenyl)amino]oxo-, ethyl ester

생성물 1

HCID 19980329HCID 19980329, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

NaH (1 g, 22 mmol) was added in portions to a stirred solution of N-ethoxalyl-2-nitro-6-methylaniline (5 g, 20 mmol) in DMF (50 ml). Methyl iodide (2 ml, 22 mmol) was thereafter added. The mixture was left overnight at room temperature, whereafter the solvent was removed by evaporation in vacuo. The residue was partitioned between ether and water. The organic phase was washed with water, dried over Na2SO4 and evaporated to give the title compound as an oil.

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후처리

  1. customwas removed by evaporation in vacuo
  2. customThe residue was partitioned between ether and water
  3. washThe organic phase was washed with water
  4. dry with materialdried over Na2SO4
  5. customevaporated

출처 및 근거

ORD 기록
ord-96a5e5041e784b8e8bfb7cb94618e03d
출처 데이터셋
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05075304

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