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N-Methyl-4-nitroaniline → 2-bromo-N-methyl-N-(4-nitrophenyl)acetamide

HRID 989401
ノート
印刷プレビュー

反応式

HRID 989401 の反応式
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-:11])=[O:10])=[CH:5][CH:4]=1.C(=O)([O-])[O-].[Li+].[Li+].[Br:18][CH2:19][C:20](Br)=[O:21]>O1CCOCC1>[Br:18][CH2:19][C:20]([N:2]([C:3]1[CH:4]=[CH:5][C:6]([N+:9]([O-:11])=[O:10])=[CH:7][CH:8]=1)[CH3:1])=[O:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7483N-Methyl-4-nitroanilineHCID 11125Lithium CarbonateHCID 61147Bromoacetyl bromide

生成物 1

HCID 226683752-bromo-N-methyl-N-(4-nitrophenyl)acetamide

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

23.5 g (0.15 mol) of N-methyl-4-nitroaniline are dissolved in 400 ml of dioxane and combined with 22.2 g (0.3 mol) of lithium carbonate. Then 32.2 g (0.18 mol) of bromoacetylbromide are added dropwise in such a way that the internal temperature does not exceed 33° C. After 18 hours' stirring the reaction solution is evaporated down to 100 ml, combined with 500 ml of water and stirred for 1 hour. The precipitate formed is suction filtered, washed with water and dried. The crude product is stirred in 400 ml of ethyl acetate at 40° C. Then the insoluble matter is filtered off, the solution is evaporated down and the solid residue is triturated with ether.

後処理

  1. customdoes not exceed 33° C
  2. customis evaporated down to 100 ml
  3. stirringstirred for 1 hour
  4. customThe precipitate formed
  5. filtrationfiltered
  6. washwashed with water
  7. customdried
  8. stirringThe crude product is stirred in 400 ml of ethyl acetate at 40° C
  9. filtrationThen the insoluble matter is filtered off
  10. customthe solution is evaporated down
  11. customthe solid residue is triturated with ether

出典と根拠

ORDレコード
ord-bea18bee3b6d4a8f80a41c8184565167
出典データセット
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06638965B2

反応ノート

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