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HRID 1164539作成日:2026年10月24日

Thionyl Chloride → HCID 20511269、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物HCID 178482014HCID 178482014—
触媒DimethylformamideHCID 6228—
溶媒BenzeneHCID 241—
生成物HCID 20511269HCID 20511269—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04370332
出典データセットuspto-grants-1983_01
ORD IDord-2a68ac0380d7430e88afa09bec913023
出典メモuspto-grants-1983_01