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Hydrogen Peroxide → 5-(3-dimethylaminopropyl)-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene

HRID 2071746
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2071746
CN(C)CCCC1C2C=C(SC)C=CC=2C=CC2C=CC=CC1=2.OO.C(O)(=O)C(O)=O.C(O)(=O)C(O)=O.[CH3:38][N:39]([CH3:62])[CH2:40][CH2:41][CH2:42][CH:43]1[C:49]2[CH:50]=[C:51]([S:54]([CH3:57])(=[O:56])=[O:55])[CH:52]=[CH:53][C:48]=2[CH:47]=[CH:46][C:45]2[CH:58]=[CH:59][CH:60]=[CH:61][C:44]1=2>C(O)C.C(O)(=O)C>[CH3:62][N:39]([CH3:38])[CH2:40][CH2:41][CH2:42][CH:43]1[C:49]2[CH:50]=[C:51]([S:54]([CH3:57])(=[O:55])=[O:56])[CH:52]=[CH:53][C:48]=2[CH:47]=[CH:46][C:45]2[CH:58]=[CH:59][CH:60]=[CH:61][C:44]1=2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 784Hydrogen PeroxideHCID 971Oxalic AcidHCID 214120975-(3-Dimethylaminopropyl)-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene hydrogen oxalateHCID 543023665-(3-dimethylaminopropyl)-3-methylmercapto-5H-dibenzo[a,d]cycloheptene

Produkt 1

HCID 214120985-(3-dimethylaminopropyl)-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176Acetic AcidLösungsmittelHCID 702EthanolLösungsmittel2×

Reaktionsbedingungen

Temperatur
15 °C

Versuchsvorschrift

5-(3-Dimethylaminopropyl)-3-methylmercapto-5H-dibenzo[a,d]cycloheptene, 1.6 g. (0.005 mole), is dissolved in 16 ml. of glacial acetic acid. The solution is cooled in an ice-bath to 15° C. and stirred while hydrogen peroxide, 2 ml. of 30%, is added dropwise. The ice-bath then is removed and the solution stirred while it warms to room temperature and then allowed to stand for 65 hours. The solution is cooled in an ice-bath and stirred while sulfur dioxide is introduced for 1 hour. After dilution with an equal mixture is rendered alkaline with sodium hydroxide and the oily base extracted into benzene. Solvent is evaporated from the washed benzene extract under reduced pressure, leaving the product as a viscous oily residue in a yield of 1.75 g. (93%). The base may be converted to the hydrogen oxalate salt by treating a solution in ethanol with an equimolar quantity of oxalic acid dissolved in ethanol. 5-(3-Dimethylaminopropyl)-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene hydrogen oxalate separates as a white crystalline solid, m.p. 191°-192° C. dec. The melting point is unchanged by recrystallization from ethanol.

Aufarbeitung

  1. dissolution(0.005 mole), is dissolved in 16 ml
  2. additionof 30%, is added dropwise
  3. customThe ice-bath then is removed
  4. customwarms to room temperature
  5. temperatureThe solution is cooled in an ice-bath
  6. stirringstirred while sulfur dioxide
  7. additionis introduced for 1 hour
  8. extractionthe oily base extracted into benzene
  9. customSolvent is evaporated from the washed benzene
  10. extractionextract under reduced pressure
  11. customleaving the product as a viscous oily residue in a yield of 1.75 g
  12. customThe melting point is unchanged by recrystallization from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-e1205eab7b554a9197ae5993915db9b5
Quelldatensatz
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04048223

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