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Acetic Acid → (+/-)-cis-6-(3,4-Dimethoxyphenyl)-cyclohex-3-enylamine

HRID 334349
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 334349
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[CH2:14][CH:13]=[CH:12][CH2:11][C@@H:10]2[N+:15]([O-])=O)=[CH:5][C:4]=1[O:18][CH3:19].C(O)(=O)C>C(O)C.[Zn]>[CH3:19][O:18][C:4]1[CH:5]=[C:6]([C@@H:9]2[C@H:10]([NH2:15])[CH2:11][CH:12]=[CH:13][CH2:14]2)[CH:7]=[CH:8][C:3]=1[O:2][CH3:1]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 176Acetic AcidHCID 15389588(+/-)-cis-1 2-Dimethoxy-4-(2-nitrocyclohex-4-enyl)benzene2×

Produkt 1

HCID 86601281(+/-)-cis-6-(3,4-Dimethoxyphenyl)-cyclohex-3-enylamineAusbeute 32,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

40 g of (±)-cis-1,2-dimethoxy-4-(2-nitrocyclohex-4-enyl)benzene (compound F7) are dissolved in 400 ml of ethanol and 40 g of zinc powder are added. After heating to boiling temperature, 65 ml of glacial acetic acid are added dropwise. Afterwards, the reaction mixture is filtrated and concentrated. The residue is redissolved in diluted hydrochloric acid and extracted with toluene. The aqueous layer is alkalized using 6 N solution of sodium hydroxide and extracted several times with toluene. The combined organic phases of the alkalic extraction are dried using sodium sulfate and concentrated. The residue is chromatographed on silica gel. 11.5 g of the title compound are obtained.

Aufarbeitung

  1. temperatureAfter heating
  2. additionare added dropwise
  3. filtrationAfterwards, the reaction mixture is filtrated
  4. concentrationconcentrated
  5. dissolutionThe residue is redissolved in diluted hydrochloric acid
  6. extractionextracted with toluene
  7. extractionextracted several times with toluene
  8. extractionThe combined organic phases of the alkalic extraction
  9. customare dried
  10. concentrationconcentrated
  11. customThe residue is chromatographed on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-c142d8147a4b46bea6095ba7276dd21c
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08883818B2

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