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Sodium Sulfate → Phenethylamine, 2,6-dichloro-4-dimethylamino-alpha-methyl-, dihydrochloride

HRID 1973279
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HRID 1973279 반응식
[CH3:1][N:2]([CH3:17])[C:3]1[CH:8]=[C:7]([Cl:9])[C:6]([CH:10]=[C:11]([N+:13]([O-])=O)[CH3:12])=[C:5]([Cl:16])[CH:4]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1.CCOCC>[ClH:9].[ClH:9].[Cl:9][C:7]1[CH:8]=[C:3]([N:2]([CH3:1])[CH3:17])[CH:4]=[C:5]([Cl:16])[C:6]=1[CH2:10][CH:11]([NH2:13])[CH3:12]
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참가 물질

6

반응물 3

HCID 24436Sodium SulfateHCID 21226445Aluminium lithium hydrideHCID 541597833,5-Dichloro-N,N-dimethyl-4-(2-nitroprop-1-en-1-yl)aniline

생성물 1

HCID 72776Phenethylamine, 2,6-dichloro-4-dimethylamino-alpha-methyl-, dihydrochloride

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

A solution of 13.7 g of N,N-dimethyl-3,5-dichloro-4-(2-nitropropenyl)aniline in 150 ml of dry tetrahydrofuran is added dropwise with stirring to 8.0 g lithium aluminum hydride in 200 ml of dry ether. The mixture is then refluxed for 4 hours. 40 ml of saturated sodium sulphate solution is added dropwise and the mixture is filtered. The filtrate is dried over anhydrous sodium sulphate and acidified with hydrogen chloride. The precipitated salt is filtered off and washed with ether. Yield: 15.2 g, m.p. 195°-197°. The product is recrystallized from aqueous ethanol-isopropyl ether. Yield: 11.9 g, m.p. 199°-200°.

후처리

  1. temperatureThe mixture is then refluxed for 4 hours
  2. filtrationthe mixture is filtered
  3. dry with materialThe filtrate is dried over anhydrous sodium sulphate
  4. filtrationThe precipitated salt is filtered off
  5. washwashed with ether
  6. customThe product is recrystallized from aqueous ethanol-isopropyl ether

출처 및 근거

ORD 기록
ord-86789328c7794cffa351a9aa7d663c7c
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03996381

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