돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274863생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/274863

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl bromideHCID 7842—
반응물Potassium CarbonateHCID 11430—
반응물5-Phenyl-1,3,4-thiadiazol-2(3H)-oneHCID 212277—
용매AcetoneHCID 180—
생성물2-Phenyl-4-propargyl-1,3,4-thiadiazolin-5-oneHCID 532368854.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05391561
출처 데이터셋uspto-grants-1995_02
ORD IDord-2b0a415ffc4d4313a86508484378e353
출처 메모uspto-grants-1995_02