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HRID 1534059作成日:2026年10月25日

Ammonium Hydroxide → 5-(3-Methylpentan-3-yl)-1,3,4-thiadiazol-2-amine

https://huagongshe.com/reaction/1534059

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Phosphorus oxychlorideHCID 24813—
反応物2-Ethyl-2-methylbutyric acidHCID 29846—
反応物ThiosemicarbazideHCID 2723789—
溶媒1,4-DioxaneHCID 31275—
生成物5-(3-Methylpentan-3-yl)-1,3,4-thiadiazol-2-amineHCID 1323426391.9%

反応条件

温度90 °C

反応手順

A solution containing 13.0 g of 2-ethyl-2-methylbutyric acid and 9.1 g of thiosemicarbazide in 125 ml of dioxane was stirred and heated to 90° C. To the stirred reaction mixture was added dropwise over thirty minutes 15.3 g of phosphorous oxychloride. Following complete addition, the reaction mixture was heated at 90° C. for six hours. The mixture was then cooled to about 30° C. and added to 100 g of ice. The aqueous mixture was made alkaline by the addition of ammonium hydroxide, and the alkaline solution was extracted several times with ethyl acetate. The extracts were combined, washed with water, dried, and the solvent was removed by evaporation under reduced pressure to afford 17.0 g of 2-amino-5-(1-ethyl-1-methylpropyl)-1,3,4-thiadiazole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05086184
出典データセットuspto-grants-1992_02
ORD IDord-4ea1cbdbc29a45deb7bf84c338cf8d2e
出典メモuspto-grants-1992_02