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HRID 274863作成日:2026年10月26日

Propargyl bromide → 2-Phenyl-4-propargyl-1,3,4-thiadiazolin-5-one

https://huagongshe.com/reaction/274863

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl bromideHCID 7842—
反応物Potassium CarbonateHCID 11430—
反応物5-Phenyl-1,3,4-thiadiazol-2(3H)-oneHCID 212277—
溶媒AcetoneHCID 180—
生成物2-Phenyl-4-propargyl-1,3,4-thiadiazolin-5-oneHCID 532368854.9%

反応手順

To the solution of 2-phenyl-1,3,4-thiadiazolin-5-one (3 g, 16.85 mmole) in dry acetone (30 ml) under nitrogen with magnetic stirring was added potassium carbonate (3 g, 22 mmole), followed by propargyl bromide (3 g, 80% in toluene, 20 mmole) at room temperature. The mixture was refluxed for one hour. The reaction mixture was cooled down to room temperature and the solid was filtered off by suction-filtration. The filtrate was diluted with ether (200 ml) and washed with water (2×50 ml) and brine. The organic layer was dried over sodium sulfate. After the drying agent was filtered off the filtrate was concentrated to about 5 ml. Hexane was added to precipitate out the product. The product was collected by suction-filtration and washed with a little hexane to afford 2 g of 2-phenyl-4-propargyl-1,3,4-thiadiazolin-5-one as a powder. m.p.=73°-75° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05391561
出典データセットuspto-grants-1995_02
ORD IDord-2b0a415ffc4d4313a86508484378e353
出典メモuspto-grants-1995_02