돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 839952생성일: 2026년 10월 24일

Sodium Hydroxide → 2-(3,5-Dichlorobenzene-1-sulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole

https://huagongshe.com/ko/reaction/839952

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium SulfiteHCID 24437—
반응물2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazoleHCID 12874685—
반응물3,5-DichlorobenzenesulfinateHCID 17950865—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(3,5-Dichlorobenzene-1-sulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazoleHCID 2032288370%

반응 단계

A solution of 75.6 g (0.6 mole) of analytically pure sodium sulfite in 300 ml of water was pre-warmed to 60°-70° C in a beaker. 122.8 g (0.5 mole) of 3,5-dichlorobenzenesulfochloride, and a solution of 40 g (1 mole) of sodium hydroxide in 200 ml of water were synchronously added dropwise from two dropping funnels in such a way that the pH value (measured with an electrode in the reaction solution) was always between 7 and 9; during the addition the mixture was stirred magnetically. The saline solution of the 3,5-dichlorobenzenesulfinate (about 600 ml) was then diluted with 1.8 liters of dimethylformamide and after adding 116.5 g (0.5 mole) of 2-bromo-5-trifluoromethyl-1,3,4-thiadiazole the whole was stirred for 15 hours at 50° C. The sulfone was precipitated completely by adding ice water and was recrystallized from ethanol. 121 g (70% of theory) of 2-(3',5'-dichlorophenylsulfonyl)-5-trifluoromethyl-1,3,4-thiadiazole of melting point 123° C were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04097669
출처 데이터셋uspto-grants-1978_06
ORD IDord-a03dd99102214b99ac881afb4d6bb399
출처 메모uspto-grants-1978_06