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Epichlorohydrin → n-[1-(4-Chlorophenyl)-1-methylethyl]-2,3-epoxypropylamine

HRID 323942
ノート
印刷プレビュー

反応式

HRID 323942 の反応式
[CH2:1]([CH:3]1[O:5][CH2:4]1)Cl.[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([NH2:16])([CH3:15])[CH3:14])=[CH:9][CH:8]=1.[OH-].[Na+]>CO>[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]([NH:16][CH2:1][CH:3]2[O:5][CH2:4]2)([CH3:14])[CH3:15])=[CH:11][CH:12]=1
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 7835EpichlorohydrinHCID 14798Sodium HydroxideHCID 110302561-(4-Chlorophenyl)-1-methylethylamine

生成物 1

HCID 18349585n-[1-(4-Chlorophenyl)-1-methylethyl]-2,3-epoxypropylamine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Epichlorohydrin (8.05 ml) was added dropwise to a solution of 1-(4-chlorophenyl)-1-methylethylamine (17.38 g) in methanol (17.5 ml) at 0° C. with stirring. The solution was warmed to ambient temperature and stirred for 48 hours. Sodium hydroxide solution (50%) (17.5 ml) was added and the mixture stirred for 15 minutes. The product was extracted with ether to give an oil which was purified by flash column chromatography on silica using petroleum ether, b.p. 40-60° C./ethyl acetate/triethylamine (8:2:1) as the mobile phase with gradually increasing amounts of ethyl acetate to give N-[1-(4-chlorophenyl)-1-methylethyl]-2,3-epoxypropylamine as an oil.

後処理

  1. stirringstirred for 48 hours
  2. stirringthe mixture stirred for 15 minutes
  3. extractionThe product was extracted with ether
  4. customto give an oil which
  5. customwas purified by flash column chromatography on silica

出典と根拠

ORDレコード
ord-8d010dca0ef24c079fbc3cbfa2152aba
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06215001B1

反応ノート

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