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Urea → (2-Methoxy-ethyl)-(4-methoxy-3-nitro-phenyl)-methyl-amine

HRID 51838
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HRID 51838 반응식
[CH3:1][O:2][CH2:3][CH2:4][N:5]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1)[CH3:6].NC(N)=O.[N+:19]([O-])([O-:21])=[O:20].[K+]>S(=O)(=O)(O)O>[CH3:1][O:2][CH2:3][CH2:4][N:5]([C:7]1[CH:8]=[CH:9][C:10]([O:13][CH3:14])=[C:11]([N+:19]([O-:21])=[O:20])[CH:12]=1)[CH3:6]
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참가 물질

5

반응물 3

HCID 1176UreaHCID 24434Potassium NitrateHCID 118437404-methoxy-N-(2-methoxyethyl)-N-methylaniline

생성물 1

HCID 22736970(2-Methoxy-ethyl)-(4-methoxy-3-nitro-phenyl)-methyl-amine수율 35.3%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

실험 절차

To a stirred solution of 600 mg (3.07 mmol) (2-methoxy-ethyl)-(4-methoxy-phenyl)-methyl-amine in 1.3 ml concentrated sulfuric acid at room temperature was added 222 mg (3.69 mmol) urea. After stirring for 1 h at room temperature, a solution of 342 mg (3.38 mmol) potassium nitrate in 0.6 ml concentrated sulfuric acid was added dropwise and stirring continued for a further 16 h. The mixture was then poured onto water amd extracted five times with dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (1/9 ethyl acetate/hexane) afforded 260 mg (35%) (2-methoxy-ethyl)-(4-methoxy-3-nitro-phenyl)-methyl-amine as an orange oil. ES-MS m/e (%): 241 (M+H+, 100).

후처리

  1. stirringstirring
  2. waitcontinued for a further 16 h
  3. additionThe mixture was then poured onto water
  4. extractionamd extracted five times with dichloromethane
  5. dry with materialThe combined organic phases were dried over sodium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f42ccbe1767f4fed8adfe048a7432cda
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06713499B2

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