戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 34424作成日:2026年10月26日

Water → 2-(2-Pinanylthio)-5-(t-butylthio)-1,3,4-thiadiazole

https://huagongshe.com/reaction/34424

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物tert-ButanolHCID 6386—
反応物(+-)-alpha-PineneHCID 6654—
反応物HCID 178418558HCID 178418558—
触媒Sulfuric AcidHCID 1118—
溶媒O-XyleneHCID 7237—
生成物2-(2-Pinanylthio)-5-(t-butylthio)-1,3,4-thiadiazoleHCID 20129852—

反応条件

温度140 °C

反応手順

2,5-Dimercapto-1,3,4-thiadiazole (35 g, 0.23 mol) and alpha-pinene (35 g, 0.26 mol) were charged to a reaction vessel and heated cautiously to 140° C. (exothermic reaction). The reaction was maintained at 135°-155° C. for 15 min. The reaction was fitted with a Dean Stark trap filled with xylene. Xylene (15 ml) was charged to the reaction. The reaction was fitted with an addition funnel containing t-butanol (25 g, 0.34 mol). The alcohol was added slowly with the reaction refluxing. Sulfuric acid (3 drops) was added to accelerate the water removal. The reaction product was isolated after approximately 5 ml (about 0.25 mol) of water were collected. Solvent was stripped by rotary evaporation. The product was mixed with calcium hydroxide (1 g), hexane (about 100 ml), and sufficient acetone (about 50 ml) to maintain one liquid layer. The product was filtered using a filter aid and the solvent removed by rotary evaporation. This afforded the final product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04761482
出典データセットuspto-grants-1988_08
ORD IDord-ba1ce414a207408996063908143efced
出典メモuspto-grants-1988_08