Dimethylformamide → N-(4-tert-pentylbenzyl)-N-methyl-1-naphthylmethylamine hydrochloride

HRID 1741735

Reaktionsgleichung

Reaktionsgleichung von HRID 1741735
[CH3:1][NH:2][CH2:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6][CH:5]=1.C(=O)([O-])[O-].[Na+].[Na+].CN(C)C=O.[C:25]([C:30]1[CH:37]=[CH:36][C:33]([CH2:34][Cl:35])=[CH:32][CH:31]=1)([CH2:28][CH3:29])([CH3:27])[CH3:26]>O>[ClH:35].[C:25]([C:30]1[CH:37]=[CH:36][C:33]([CH2:34][N:2]([CH2:3][C:4]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[CH:7]=[CH:6][CH:5]=2)[CH3:1])=[CH:32][CH:31]=1)([CH2:28][CH3:29])([CH3:27])[CH3:26]

Komponenten

6

Versuchsvorschrift

To a mixture of 1.03 g of N-methyl-1-naphthylmethylamine, 0.7 g of sodium carbonate and 10 ml of dimethylformamide was added 1.3 g of 4-tert-pentylbenzyl chloride and was stirred at room temperature for 16 hours. The reaction mixture was poured into water and extracted with benzene, and the benzene solution was washed with water. After distilling away benzene, 1.5 ml of concentrated hydrochloric acid was added and then an excess of concentrated hydrochloric acid was removed. A small amount of acetone was added and 1.33 g of formed white crystal was filtrated. White crystal of N-(4-tert-pentylbenzyl)-N-methyl-1-naphthylmethylamine hydrochloride (Compound of Example 12) was obtained by recrystallization from acetone.

Aufarbeitung

  1. extractionextracted with benzene
  2. washthe benzene solution was washed with water
  3. distillationAfter distilling away benzene, 1.5 ml of concentrated hydrochloric acid
  4. additionwas added
  5. customan excess of concentrated hydrochloric acid was removed
  6. additionA small amount of acetone was added
  7. filtration1.33 g of formed white crystal was filtrated

Quellen und Nachweise

ORD-Eintrag
ord-2df96ef726e9474bad41f2ba8af3e716
Quelldatensatz
uspto-grants-1994_08
Patentnummer
US05334628

Verknüpfte Notizen

Wird geladen…