Hydroquinone → (+/-)-trans-1,2-DI methoxy-4-(2-nitrocyclohex-4-enyl)benzene

HRID 30076

Reaktionsgleichung

Reaktionsgleichung von HRID 30076
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][C:13]=1[O:14][CH3:15])[CH:6]=[CH:7][N+:8]([O-:10])=[O:9].[C:16]1([CH:23]=CC(O)=[CH:19][CH:18]=1)O.C=CC=C>C1(C)C=CC=CC=1>[CH3:15][O:14][C:13]1[CH:12]=[CH:11][C:5]([C@@H:6]2[CH2:19][CH:18]=[CH:16][CH2:23][C@H:7]2[N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[O:2][CH3:1]

Komponenten

5

Edukt 3

HCID 785HydroquinoneHCID 78451,3-ButadieneHCID 2220933,4-Dimethoxy-beta-nitrostyrene

Produkt 1

HCID 53874256(+/-)-trans-1,2-DI methoxy-4-(2-nitrocyclohex-4-enyl)benzene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

50.0 g of 3,4-dimethoxy-nitrostyrene (compound J1), and 1.0 g (9.1 mmol) of hydroquinone are suspened in 200 ml of abs. toluene and treated at −70° C. with 55.0 g (1.02 mol) of liquid 1,3-butadiene. The mixture is stirred at 160° C. for 6 days in an autoclave and then cooled. Some of the solvent is removed on a rotary evaporator, and the resulting precipitate is filtered off with suction and recrystallized in ethanol. M.p.: 113.5-115.5° C.

Aufarbeitung

  1. temperaturecooled
  2. customSome of the solvent is removed on a rotary evaporator
  3. filtrationthe resulting precipitate is filtered off with suction
  4. customrecrystallized in ethanol

Quellen und Nachweise

ORD-Eintrag
ord-0d9c619fbf6e475e9d00cefe1466429a
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07423046B2

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