戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 260539作成日:2026年10月25日

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

https://huagongshe.com/reaction/260539

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物tert-Butyl hydroperoxideHCID 6410—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物1,2,5-Thiadiazole-3,4-dicarboxylic acidHCID 270016—
反応物DiaminomaleonitrileHCID 2723951—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物3,4-Di(t-butylperoxycarbonyl)-1,2,5-thiadiazoleHCID 19977652—

反応手順

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##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05527921
出典データセットuspto-grants-1996_06
ORD IDord-22b50df7327346b88708c74ba16c6802
出典メモuspto-grants-1996_06