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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1164539생성일: 2026년 10월 24일

Thionyl Chloride → HCID 20511269, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물HCID 178482014HCID 178482014—
촉매DimethylformamideHCID 6228—
용매BenzeneHCID 241—
생성물HCID 20511269HCID 20511269—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04370332
출처 데이터셋uspto-grants-1983_01
ORD IDord-2a68ac0380d7430e88afa09bec913023
출처 메모uspto-grants-1983_01