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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239033생성일: 2026년 10월 25일

Cyclohexanethiol → 2-(Cyclohexylthio)-6-(trifluoromethyl)nicotinonitrile

https://huagongshe.com/reaction/239033

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanethiolHCID 15290—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물2-Chloro-6-(trifluoromethyl)nicotinonitrileHCID 2778413—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(Cyclohexylthio)-6-(trifluoromethyl)nicotinonitrileHCID 5982686394.6%

반응 단계

1.3 Equivalents of NaH (4.9 g, 0.124 mol) were dissolved in 50 mL of DMF under a blanket of nitrogen. Following the addition of 1.2 equivalents of cyclohexanethiol (14.2 mL, 0.116 mol), the mixture was stirred at RT over a period of 1.5 h. The resulting suspension was cooled to 10° C. and added dropwise to 1 equivalent of 2-chloro-6-(trifluoromethyl)nicotinonitrile (20 g, 0.096 mol) in 50 mL of DMF and stirred over a period of 2 h at RT. To the reaction mixture there was added sat. aq. NH4Cl soln. and the mixture was diluted with 1 L of water and extracted with EA (3×200 mL). The combined organic phases were washed with sat. aq. NaCl solution, dried over MgSO4 and concentrated in vacuo. Column chromatographic purification (silica gel 100-200 mesh, eluant: 2% EA in hexane) yielded 26 g (93.8%) of product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642775B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-5b3a03f7e2f541cd9acbddc0aaec5a1b
출처 메모uspto-grants-2014_02