Hydrochloric Acid → 5-(3-Dimethylaminopropyl)-5H-dibenzo[a,d]cycloheptene hydrochloride

HRID 1284234Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1284234
[CH3:1][N:2]([CH3:8])[CH2:3][CH2:4][CH2:5][Mg][Cl:7].Cl[CH:10]1[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[CH:14]=[CH:13][C:12]2[CH:21]=[CH:22][CH:23]=[CH:24][C:11]1=2.O1CCCC1.Cl>CCOCC>[ClH:7].[CH3:1][N:2]([CH3:8])[CH2:3][CH2:4][CH2:5][CH:10]1[C:11]2[CH:24]=[CH:23][CH:22]=[CH:21][C:12]=2[CH:13]=[CH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]1=2

Komponenten

6

Edukt 4

HCID 313Hydrochloric Acid2×HCID 8028TetrahydrofuranHCID 110751355-Chloro-5H-dibenzo[a,d][7]annuleneHCID 178483494HCID 178483494, Verbindung

Produkt 1

HCID 681195605-(3-Dimethylaminopropyl)-5H-dibenzo[a,d]cycloheptene hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

The Grignard solution prepared in Step A. is cooled to room temperature and stirred while a solution of 5.05 g. (0.0221 mole) of 5-chloro-5H-dibenzo[a,d]cycloheptene in 25 ml. of dry tetrahydrofuran is added dropwise, external cooling being applied as required to maintain the temperature close to room temperature. When the addition is complete, the mixture is heated to refluxing for 15 minutes. The bulk of the tetrahydrofuran then is distilled under reduced pressure, keeping the water-bath temperature at 50°-60°C. The syrupy mixture is dissolved in 75 ml. of benzene and water, 15 ml., is added dropwise with stirring. The benzene layer is decanted from the gelatinous precipitate which then is re-extracted with three 20 ml. portions of boiling benzene. The combined benzene extracts are washed with water and extracted with three 15 ml. portions of 3N hydrochloric acid. The acid extract is made basic with sodium hydroxide and the yellow oily base that separates is extracted into hexane. After washing the combined extracts with water, the hexane is evaporated and the product obtained as a yellow oil in a yield of 4.61 g. The base is converted to the hydrochloride by dissolving it in a mixture of 15 ml. of absolute alcohol and 15 ml. of absolute ether and adding 1.8 ml. of a 10.28 N solution of dry hydrogen chloride in absolute alcohol. The solution then is diluted to incipient crystallization by the addition of 25 ml. of absolute ether. The yield of 5-(3-dimethylaminopropyl)-5H-dibenzo[a,d]cycloheptene hydrochloride, m.p. 186°-190°C. is 4.17 g. Recrystallization from mixtures of absolute alcohol and absolute ether gives the product, m.p. 191°-193°C.

Aufarbeitung

  1. temperatureexternal cooling
  2. temperatureto maintain the temperature
  3. customclose to room temperature
  4. additionWhen the addition
  5. temperaturethe mixture is heated
  6. temperatureto refluxing for 15 minutes
  7. distillationThe bulk of the tetrahydrofuran then is distilled under reduced pressure
  8. customat 50°-60°C
  9. dissolutionThe syrupy mixture is dissolved in 75 ml
  10. addition, is added dropwise
  11. stirringwith stirring
  12. customThe benzene layer is decanted from the gelatinous precipitate which
  13. extractionthen is re-extracted with three 20 ml
  14. washThe combined benzene extracts are washed with water
  15. extractionextracted with three 15 ml
  16. extractionThe acid extract
  17. extractionthe yellow oily base that separates is extracted into hexane
  18. washAfter washing the combined extracts with water
  19. customthe hexane is evaporated
  20. customthe product obtained as a yellow oil in a yield of 4.61 g
  21. dissolutionby dissolving it
  22. additionin a mixture of 15 ml
  23. additionThe solution then is diluted
  24. customcrystallization
  25. additionby the addition of 25 ml
  26. customRecrystallization from mixtures of absolute alcohol and absolute ether
  27. customgives the product, m.p. 191°-193°C.

Quellen und Nachweise

ORD-Eintrag
ord-9eaea52bcc9d40af819e05249f7ef0e2
Quelldatensatz
uspto-grants-1976_08
Patentnummer
US03978121

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