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

HRID 378602
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HRID 378602 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7835EpichlorohydrinHCID 14798Sodium HydroxideHCID 110302561-(4-Chlorophenyl)-1-methylethylamine

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-9f5bbae335b341e39649641d7c9b9188
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06031109

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