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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375817생성일: 2026년 10월 25일

Cyanogen Bromide → 4-Phenyl-3-thiocyanato-1,2,5-thiadiazole

https://huagongshe.com/reaction/375817

반응식

참여 물질

역할이름HCID투입량
반응물Cyanogen BromideHCID 10476—
반응물Sodium SulfideHCID 14804—
반응물3-Chloro-4-phenyl-1,2,5-thiadiazoleHCID 2764044—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-Phenyl-3-thiocyanato-1,2,5-thiadiazoleHCID 15337497—

반응 단계

To a stirred solution of 3.8 grams(g)(0.05 mole) of sodium sulfide in 100 mL of dimethylformamide was added 8 g(0.041 mole) of 4-Phenyl-3-chloro-1,2,5-thiadiazole. The mixture was stirred overnight (~16 hours), and to the resulting dark green solution was added 6.64 g(1.5 molar equivalents) of cyanogen bromide. This mixture was stirred for about 14 hours and then diluted with 100 mL of water and extracted with 200 mL of methylene chloride. The organic layer was separated and washed with water (2×100 mL), dried and concentrated under reduced pressure. The thus recovered crude material was chromatographed on silica gel with a 10% EtoAc:90% hexane mixture to yield 6.6 g (72 percent of theoretical) as an oil which turned to a white solid melting at 49° C. upon standing; 13C NMR (75 MHz, CDCl3) δ 159.10, 141.78, 130.59, 129.76, 129.06, 127.88, 105.98; MS (EI) m/e 219(M+), 192, 160, 135, 103.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05488060
출처 데이터셋uspto-grants-1996_01
ORD IDord-b1f292df84a140e38b591869d9253f42
출처 메모uspto-grants-1996_01