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HRID 2179876作成日:2026年10月26日

Ethanol → 2-(2-Methylpentylthio)-1,3,4-thiadiazole-5-amine

https://huagongshe.com/reaction/2179876

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium HydroxideHCID 14798—
反応物2-Methyl-1-pentyl methanesulfonateHCID 22486761—
反応物HCID 178509208HCID 178509208—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2-Methylpentylthio)-1,3,4-thiadiazole-5-amineHCID 22486760—

反応手順

A three-necked 3-L round bottom flask was charged with 2-methylpentyl methanesulphonate (90 g, 0.5 mol), ethanol (1.5 L) and 2-mercapto-1,3,4-thiadiazole-5-amine (66.5 g, 0.5 mol). Sodium hydroxide (20 g, 0.5 mol) was added to the stirred suspension. The mixture was heated to reflux and held at reflux over night. As the mixture warmed the cream suspension gradually dissolved. Just before refluxing began a cloudy precipitate formed. The reaction mixture was cooled to room temperature, filtered, and the residue was washed well with ethanol. The resulting filtrate was concentrated to dryness to give an off-white solid that was dissolved in ethyl acetate (1.2 L) and washed with 1) water (800 mL) and 2) brine (1 L). The filtrate was dried (MgSO4) and concentrated to dryness. An off-white solid was obtained that was recrystallised from boiling acetonitrile (150 mL). The filtered material was washed well with acetonitrile and dried (Vac/40° C.). The required product was obtained as a white solid wt 83 g; 76.5%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06887656B2
出典データセットuspto-grants-2005_05
ORD IDord-35b097b0764b4dc9a89fcac955e74450
出典メモuspto-grants-2005_05