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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3620생성일: 2026년 10월 24일

Propargyl bromide → 2-(t-Butyl)-5-(2,6-dichloro-4-pyridyl)-4-propargyl-1,2,4-triazolin-3-one

https://huagongshe.com/ko/reaction/3620

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl bromideHCID 7842—
반응물Potassium CarbonateHCID 11430—
반응물2-(t-Butyl)-5-(2,6-dichloro-4-pyridyl)-1,2,4-triazolin-3-oneHCID 136351275—
촉매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(t-Butyl)-5-(2,6-dichloro-4-pyridyl)-4-propargyl-1,2,4-triazolin-3-oneHCID 86752341—

반응 단계

To 2.06 g (7.2 mmol) of crude 2-(t-butyl)-5-(2,6-dichloro-4-pyridyl)-1,2,4-triazolin-3-one were added 30 mL of ethyl acetate, 1 drop of water, and 1.00 g (7.30 mmol) of powdered K2CO3. The mixture was heated to reflux and after 15 min 1.10 g (7.4 mmol) of an 80% by weight solution of propargyl bromide in toluene was added. Refluxing was continued for 2.5 hours. The mixture was cooled, diluted with 175 mL of ethyl acetate, washed with 25 mL of water, and dried over MgSO4. Reomoval of the solvent left 2.18 g of crude product as a reddish solid. The crude product was combined with 0.69 g of material from another run and purified by flash chromatography first on a silica gel column and then on a neutral alumina column eluted portionwise in both cases with ether hexane mixtures containing successively greater percentages of ether to afford 0.97 g of 2-(t-butyl)-5-(2,6-dichloro-4-pyridyl)-4-propargyl-1,2,4-triazolin-3-one (Compound 1) as a white solid, m.p. 107°-109° C. 1H-NMR (CDCl3)∂1.6 (9H,s), 2.45 (1H,t), 4.6 (2H,d), 7.75 (2H,s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733849
출처 데이터셋uspto-grants-1998_03
ORD IDord-88c4d02c8563491e94268fb63352bd18
출처 메모uspto-grants-1998_03