Dimethylamine → 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole

HRID 268524

Reaktionsgleichung

Reaktionsgleichung von HRID 268524
Cl[CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:8]=[CH:9][C:10]2[N:11]([CH2:26][CH3:27])[C:12]3[C:17]([C:18]=2[CH:19]=1)=[CH:16][C:15]([C:20](=[O:25])[CH2:21][CH2:22][CH2:23]Cl)=[CH:14][CH:13]=3)=[O:6].C([N:30]1[C:42]2C=CC=CC=2C2[C:31]1=CC=CC=2)C.ClCCCC(Cl)=O.[CH3:50][NH:51][CH3:52].[I-].[K+].[C:55]([OH:62])(=[O:61])/[CH:56]=[CH:57]/[C:58]([OH:60])=[O:59]>O1CCOCC1>[CH3:50][N:51]([CH3:52])[CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:8]=[CH:9][C:10]2[N:11]([CH2:26][CH3:27])[C:12]3[C:17]([C:18]=2[CH:19]=1)=[CH:16][C:15]([C:20](=[O:25])[CH2:21][CH2:22][CH2:23][N:30]([CH3:42])[CH3:31])=[CH:14][CH:13]=3)=[O:6].[C:55]([O-:62])(=[O:61])/[CH:56]=[CH:57]/[C:58]([O-:60])=[O:59]

Komponenten

9

Edukt 6

HCID 674DimethylamineHCID 4875Potassium IodideHCID 6836N-ethyl carbazoleHCID 783704-Chlorobutyryl chlorideHCID 444972Fumaric AcidHCID 123317903,6-Bis(4-chlorobutyryl)-N-ethylcarbazole

Produkt 2

HCID 4613193,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazoleHCID 5460307Fumarate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

A mixture of 15.8 g (0.039 mole) of 3,6-bis(4-chlorobutyryl)-N-ethylcarbazole, prepared from N-ethylcarbazole and 4-chlorobutyryl chloride, 75 ml of 40% aqueous dimethylamine and 2 g of potassium iodide in 175 ml of p-dioxane is heated in a reaction bomb with stirring for 44 hours. The reaction mixture is concentrated to one-half its original volume in vacuo and diluted with 500 ml of water. The semi-solid which separates is dissolved in ether and washed repeatedly with water and dried over magnesium sulfate to give the free base which is treated with fumaric acid and recrystallized from butanone to give 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole bis acid fumarate. M.P. 94°-98°C.

Aufarbeitung

  1. temperatureis heated in a reaction bomb
  2. concentrationThe reaction mixture is concentrated to one-half its original volume in vacuo
  3. additiondiluted with 500 ml of water
  4. dissolutionThe semi-solid which separates is dissolved in ether
  5. washwashed repeatedly with water
  6. dry with materialdried over magnesium sulfate
  7. customto give the free base which
  8. customrecrystallized from butanone

Quellen und Nachweise

ORD-Eintrag
ord-98dbf57019ff4ad687fba3e1257f67bf
Quelldatensatz
uspto-grants-1976_03
Patentnummer
US03947593

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