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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2116663생성일: 2026년 10월 26일

Iodoethylene → 1,1,1-Trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)but-3-en-2-ol

https://huagongshe.com/reaction/2116663

반응식

참여 물질

역할이름HCID투입량
반응물IodoethyleneHCID 68976—
반응물HCID 178418306HCID 178418306—
반응물HCID 178519847HCID 178519847—
용매Diethyl EtherHCID 3283—
생성물1,1,1-Trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)but-3-en-2-olHCID 178458803—

반응 조건

온도-78 °C

반응 단계

To a solution of vinyl iodide (1.88 g, 12.2 mmol) in Et2O at −78° C. was added t-butyl lithium (14.3 ml, 1.7 M/pentane, 24.3 mmol). The mixture was stirred at −78° C. for 1 h and warmed up to −30° C. for 5 min. The mixture was cooled back to −78° C. and 2,2,2-trifluoro-1-(2-mercapto-1,3-thiazol-5-yl)ethanone (1.18 g, 5.53 mmol) in Et2O was added. The reaction mixture stirred 30 min at −78° C., brought to 0° C. and partitioned between aqueous NH4Cl and EtOAc. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated and the residue chromatographed on silica gel (toluene/acetone; 90:10) to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07439260B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-6688bbe9cb174e38b23a8b7707a6b987
출처 메모uspto-grants-2008_10