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Methyl iodide → N,5-Dimethyl-2-nitroaniline

HRID 885455
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HRID 885455 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:9]([O-:11])=[O:10])=[C:6]([NH2:8])[CH:7]=1.[H-].[Na+].I[CH3:15]>CN(C=O)C>[CH3:15][NH:8][C:6]1[CH:7]=[C:2]([CH3:1])[CH:3]=[CH:4][C:5]=1[N+:9]([O-:11])=[O:10]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 113566-Nitro-m-toluidineHCID 24758Sodium hydride

생성물 1

HCID 10103510N,5-Dimethyl-2-nitroaniline

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a solution of 5-methyl-2-nitro-phenylamine (3.04 g, 20.0 mmol) in anhydrous DMF (20 mL) at 0° C. was portionwise added 95% NaH (528 mg, 22.0 mmol) and stirred for 10 min. A solution of iodomethane (1.25 mL, 20.0 mmol) in anhydrous DMF (10 mL) was then added. The ice bath was removed and the resulting mixture was stirred at room temperature overnight. The resulting mixture was then diluted with water, and the resulting solid was collected by filtration, washed with H2O and hexanes to yield methyl-(5-methyl-2-nitro-phenyl)-amine MS 167 (M+1)+.

후처리

  1. customat 0° C.
  2. customThe ice bath was removed
  3. stirringthe resulting mixture was stirred at room temperature overnight
  4. additionThe resulting mixture was then diluted with water
  5. filtrationthe resulting solid was collected by filtration
  6. washwashed with H2O and hexanes

출처 및 근거

ORD 기록
ord-380a6d8fad4947eca7795d184e2fa4b9
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242157B2

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