돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260539생성일: 2026년 10월 24일

Toluene → 3,4-Di(t-butylperoxycarbonyl)-1,2,5-thiadiazole

https://huagongshe.com/ko/reaction/260539

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물tert-Butyl hydroperoxideHCID 6410—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물1,2,5-Thiadiazole-3,4-dicarboxylic acidHCID 270016—
반응물DiaminomaleonitrileHCID 2723951—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물3,4-Di(t-butylperoxycarbonyl)-1,2,5-thiadiazoleHCID 19977652—

반응 단계

The preparation described in Warren, J. D., et al, J. Heterocyclic Chem. 16, 1817 (1979) was used to prepare 1,2,5-thiadiazole-3,4-dicarboxylic acid from diaminomaleonitrile. At room temperature, 4.30 g of p-toluenesulfonyl chloride was added to a solution of 0.990 g of 1,2,5-thiadiazole-3,4-dicarboxylic acid in 10 mL of pyridine. The solution was cooled in an ice bath and 1.09 g of t-butylhydroperoxide (90% solution in water) was added. The solution was stirred for one hour during which it was cooled with an ice bath such that the temperature was as low as possible without freezing the pyridine. The solution was then poured into a mixture of water and toluene. The toluene layer was separated and washed twice with a 10% aqueous sodium hydroxide solution. The toluene solution was then dried over sodium sulfate and the solvents removed giving rise to 1.414 g of a yellow liquid. The yellow liquid was purified by column chromatography to give a colorless solid with a melting point of 39°-41° C.; 1H NMR (CDCl3) δ 1.42 (s); IR (coated on a thin polymer film) 1784, 1132, 1019 cm-1. ##STR17##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05527921
출처 데이터셋uspto-grants-1996_06
ORD IDord-22b50df7327346b88708c74ba16c6802
출처 메모uspto-grants-1996_06