Thionyl Chloride → HCID 20511269, Verbindung

HRID 1284065

Reaktionsgleichung

Reaktionsgleichung von HRID 1284065
[CH3:1][N:2]1[C:6]([CH2:7][C:8](O)=[S:9])=[N:5][N:4]=[N:3]1.S(Cl)([Cl:13])=O>C1C=CC=CC=1.CN(C)C=O>[CH3:1][N:2]1[C:6]([CH2:7][C:8]([Cl:13])=[S:9])=[N:5][N:4]=[N:3]1

Komponenten

5

Versuchsvorschrift

To a suspension of (1-methyl-1H-tetrazol-5-yl)-thioacetic acid (10g) in dried benzene (100 ml) were added a solution of thionyl chloride (10.2 g) in dried benzene (30 ml) and dimethylformamide (1 drop) in turn at room temperature, and the mixture was refluxed for 1 hour. After the reaction, the solvent was distilled off to give crystals of (1-methyl-1H-tetrazol-5-yl)thioacetyl chloride. To a solution of 3,4-dibenzyloxyphenethylamine (9.3 g) in a mixture of dried benzene (90 ml) and dried chloroform (10 ml) was firstly added triethylamine (3.66 g) and then was dropwise added over 20 minutes over stirring and ice cooling a solution of the above obtained (1-methyl-1H-tetrazol-5-yl)-thioacetyl chloride in a mixture of dried benzene (50 ml) and dried chloroform (5 ml). The mixture was stirred for 30 minutes at the same temperature and for 30 minutes at room temperature. The solvent was distilled off and the residue was dissolved in chloroform. The solution was in turn washed with 5% hydrochloric acid, water, dilute sodium bicarbonate aqueous solution and water and dried. The solvent was distilled off and the residue was crystallized from ether to give N-(3,4-dibenzyloxyphenethyl)-(1-methyl-1H-tetrazol-5-yl)-thioacetamide (10.7 g), mp 110°C.

Aufarbeitung

  1. temperaturethe mixture was refluxed for 1 hour
  2. customAfter the reaction
  3. distillationthe solvent was distilled off

Quellen und Nachweise

ORD-Eintrag
ord-0da7e6f3a68e4550a6e9ec7206f7cf46
Quelldatensatz
uspto-grants-1976_08
Patentnummer
US03978063

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