Sodium hydride → 2-Benzoyl-1-cyano-5,7-dibenzyloxy-1-(3,4,5-trimethoxybenzyl)-1,2-dihydroisoquinoline

HRID 973040

Reaktionsgleichung

Reaktionsgleichung von HRID 973040
[H-].[Na+].[C:3]([N:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][C:15]([O:29][CH2:30][C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)=[CH:16][C:17]=2[O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:12]1[C:37]#[N:38])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:39][O:40][C:41]1[CH:42]=[C:43]([CH:46]=[C:47]([O:51][CH3:52])[C:48]=1[O:49][CH3:50])[CH2:44]Cl>CN(C)C=O>[C:3]([N:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][C:15]([O:29][CH2:30][C:31]3[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=3)=[CH:16][C:17]=2[O:21][CH2:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[C:12]1([C:37]#[N:38])[CH2:44][C:43]1[CH:46]=[C:47]([O:51][CH3:52])[C:48]([O:49][CH3:50])=[C:41]([O:40][CH3:39])[CH:42]=1)(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 774485-(Chloromethyl)-1,2,3-trimethoxybenzeneHCID 127070612-Benzoyl-1-cyano-5,7-dibenzyloxy-1,2-dihydroisoquinoline

Produkt 1

HCID 214033662-Benzoyl-1-cyano-5,7-dibenzyloxy-1-(3,4,5-trimethoxybenzyl)-1,2-dihydroisoquinoline

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel3×

Versuchsvorschrift

Sodium hydride (prepared by washing 553 mg of 65% sodium hydride with absolute n-hexane) is suspended in 15 ml of dimethylformamide. A solution of 3.4 g of 2-benzoyl-1-cyano-5,7-dibenzyloxy-1,2-dihydroisoquinoline in 40 ml of dimethylformamide is added dropwise to the suspension at -10° C in a nitrogen atmosphere. Then, a solution of 1.71 g of 3,4,5-trimethoxybenzyl chloride in 40 ml of dimethylformamide is added dropwise to the mixture for 30 minutes, and the mixture is allowed to stand at the same temperature for 30 minutes. The reaction mixture is poured into ice-water, and extracted with ethyl acetate. The extract is evaporated to remove solvent, whereby 2-benzoyl-1-cyano-5,7-dibenzyloxy-1-(3,4,5-trimethoxybenzyl)-1,2-dihydroisoquinoline is obtained as a crude oil. The crude oil is dissolved in 200 ml of dioxane. 50 ml of an aqueous 10% sodium hydroxide solution are added to the dioxane solution, and this mixture is stirred at 50° C for 12 hours. After the reaction, the mixture is evaporated under reduced pressure to remove solvent. The residue thus obtained is extracted with methylene chloride. The methylene chloride extract is washed with water, dried and then evaporated to remove solvent. 3.1 g of 5,7-dibenzyloxy-1-(3,4,5-trimethoxybenzyl)-isoquinoline are obtained as a crude product. Yield: 84% M.p. 158° - 160° C (recrystallized from ethanol).

Aufarbeitung

  1. extractionextracted with ethyl acetate
  2. customThe extract is evaporated
  3. customto remove solvent

Quellen und Nachweise

ORD-Eintrag
ord-9d42084bfcd34c29bbef0297758fb546
Quelldatensatz
uspto-grants-1977_10
Patentnummer
US04054659

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