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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1164539Erstellt: 23. Oktober 2026

Thionyl Chloride → HCID 20511269, Verbindung

https://huagongshe.com/de/reaction/1164539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
EduktHCID 178482014HCID 178482014—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelBenzeneHCID 241—
ProduktHCID 20511269HCID 20511269—

Reaktionsschritte

To a suspension of (1-methyl-1H-tetrazol-5-yl)thioacetic acid (10 g) 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 under 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04370332
Quelldatensatzuspto-grants-1983_01
ORD IDord-2a68ac0380d7430e88afa09bec913023
Quellennotizuspto-grants-1983_01