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Toluene → Propanamide, 2-bromo-N-(2-ethyl-6-methylphenyl)-

HRID 1732244
ノート
印刷プレビュー

反応式

HRID 1732244 の反応式
[OH-].[Na+].[CH2:3]([C:5]1(C)[CH:11]=[CH:10][CH:9]=[CH:8][CH:6]1[NH2:7])[CH3:4].[Br:13][CH:14]([CH3:18])[C:15](Br)=[O:16].[C:19]1(C)C=CC=CC=1>>[Br:13][CH:14]([CH3:18])[C:15]([NH:7][C:6]1[C:8]([CH3:19])=[CH:9][CH:10]=[CH:11][C:5]=1[CH2:3][CH3:4])=[O:16]
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 4

HCID 1140TolueneHCID 14798Sodium HydroxideHCID 79047Propanoyl bromide, 2-bromo-HCID 20305842HCID 20305842、化合物

生成物 1

HCID 4392336Propanamide, 2-bromo-N-(2-ethyl-6-methylphenyl)-

実験手順

To a two-phase system, containing an aqueous sodium hydroxide solution (20 g sodium hydroxide in 200 ml water) and a mixture of 13.5 g 2-ethyl-2-methylaniline and 75 ml toluene (cooled to 8° C.), was added dropwise with stirring 25 g 2-bromopropionyl bromide. After this addition, stirring was continued for 15 min. and the formed crystals were filtered off. (Addition of petroleum ether to the filtrate precipitates more product, which can be added to the first crop). Total yield 22.8 g (84%). After recrystallization from ether-petroleum ether, it melted at 181°-182° C.

後処理

  1. additionwas added dropwise
  2. additionAfter this addition
  3. filtrationthe formed crystals were filtered off
  4. custom(Addition of petroleum ether to the filtrate precipitates more product, which
  5. additioncan be added to the first crop)
  6. customAfter recrystallization from ether-petroleum ether, it melted at 181°-182° C.

出典と根拠

ORDレコード
ord-d0989d1d30f14bc39066ee4fa25aa277
出典データセット
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04237068

反応ノート

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