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2-Methoxyethylamine → N-(2-Methoxyethyl)-2-nitroaniline

HRID 1460374
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HRID 1460374 반응식
F[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].[CH3:11][O:12][CH2:13][CH2:14][NH2:15]>C(O)CCC>[CH3:11][O:12][CH2:13][CH2:14][NH:15][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9]
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참가 물질

4

반응물 2

HCID 80182-MethoxyethylamineHCID 738951-Fluoro-2-nitrobenzene

생성물 1

HCID 10375425N-(2-Methoxyethyl)-2-nitroaniline

시약·촉매·용매 1

HCID 2631-Butanol용매2회

실험 절차

To 28.2g of 2-fluoronitrobenzene in 70ml of n-butanol 30.0g of 2-methoxyethylamine were added and the mixture refluxed overnight to give a dark red solution. After cooling the n-butanol was evaporated off and the product extracted into diethyl ether. The diethyl ether was then washed twice with dilute (aqueous) hydrochloric acid, once with dilute (aqueous) sodium carbonate and once with brine. The ether was then dried using magnesium sulphate and evaporated off to give 35g of 2-(2-methoxyethylamino)nitrobenzene as a red liquid.

후처리

  1. temperaturethe mixture refluxed overnight
  2. customto give a dark red solution
  3. customwas evaporated off
  4. extractionthe product extracted into diethyl ether
  5. washThe diethyl ether was then washed twice
  6. additionwith dilute (aqueous) hydrochloric acid
  7. additiononce with dilute (aqueous) sodium carbonate
  8. dry with materialThe ether was then dried
  9. customevaporated off

출처 및 근거

ORD 기록
ord-83356119afc449c09c359af5f5aa06fc
출처 데이터셋
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05071468

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