Carbon Disulfide → 2-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene

HRID 1940692

Reaktionsgleichung

Reaktionsgleichung von HRID 1940692
[CH2:1]([C:7]1[CH:12]=C[CH:10]=[CH:9][CH:8]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[Cl-].[Al+3].[Cl-].[Cl-].Cl[C:18]([CH3:26])([CH2:20][CH2:21][C:22](Cl)([CH3:24])[CH3:23])[CH3:19].[C:27](=S)=S>>[CH3:19][C:18]1([CH3:26])[C:10]2[C:23](=[CH:12][C:7]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[CH:8][CH:9]=2)[C:22]([CH3:27])([CH3:24])[CH2:21][CH2:20]1

Komponenten

5

Edukt 4

HCID 6348Carbon DisulfideHCID 14109HexylbenzeneHCID 80360Hexane, 2,5-dichloro-2,5-dimethyl-HCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 230025302-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

83 ml of hexylbenzene were treated with 1.8 g of aluminum chloride while cooling with ice. After brief stirring a solution of 40 g of 2,5-dichloro-2,5-dimethyl-hexane in 300 ml of carbon disulphide was added dropwise and the mixture was stirred at 0° C. for a further 2 hours. The reaction mixture was poured into ice/6N hydrochloric acid, extracted with ethyl acetate, dried over sodium sulphate and evaporated. The crude product was distilled in a high vacuum. There were obtained 25.5 g of 1,1,4,4-tetramethyl-6-hexyl-1,2,3,4-tetrahydro-naphthalene as a colourless oil, boiling point 141°-152° C./0.8 mm.

Aufarbeitung

  1. temperaturewhile cooling with ice
  2. additionwas added dropwise
  3. extractionextracted with ethyl acetate
  4. dry with materialdried over sodium sulphate
  5. customevaporated
  6. distillationThe crude product was distilled in a high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-24d938896b1143d190b5f80957207c08
Quelldatensatz
uspto-grants-1997_12
Patentnummer
US05700836

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