戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1073793作成日:2026年10月25日

1-Bromoheptane → 1,3,4-Thiadiazole, 2-amino-5-(heptylthio)-

https://huagongshe.com/reaction/1073793

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromoheptaneHCID 12369—
反応物Sodium HydroxideHCID 14798—
反応物HCID 178509208HCID 178509208—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1,3,4-Thiadiazole, 2-amino-5-(heptylthio)-HCID 53445882.5%

反応条件

温度60 °C

反応手順

In 185 ml of ethanol and 185 ml of water, 68.0 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 22.4 g of sodium hydroxide were added. To this mixture, 84.6 g of 1-bromoheptane was added, and the resulting mixture was warmed to 60° C. and stirred for 2 hours. After cooling, water was added and the mixture was filtered. The residue was washed with water, dried under reduced pressure, and recrystallized from an ethanol/hexane mixture. Thus 90.2 g of 2-amino-5-heptylthio-1,3,4-thiadiazole was obtained. m.p. 112°~113° C. Yield 78%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04971971
出典データセットuspto-grants-1990_11
ORD IDord-3e39365279be437890d2df62cf84d2c9
出典メモuspto-grants-1990_11