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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 568772생성일: 2026년 10월 25일

Methyl iodide → bis(4-Fluorophenyl)methyl(5-methylthiocarbonyl-1H-1,2,4-triazol-1-ylmethyl)silane

https://huagongshe.com/reaction/568772

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Carbonyl SulfideHCID 10039—
반응물Ammonium ChlorideHCID 25517—
반응물FlusilazoleHCID 73675—
용매TetrahydrofuranHCID 8028—
생성물bis(4-Fluorophenyl)methyl(5-methylthiocarbonyl-1H-1,2,4-triazol-1-ylmethyl)silaneHCID 54514882—

반응 단계

To a -78° C. solution of 0.016 mol of lithio[bis(4-fluorophenyl)methyl(1H-1,2,4-triazol-1-ylmethyl)silane, prepared in 75 mL of THF as described in Example 1, was added 1 mL of liquid carbonyl sulfide. The solution was allowed to warm to 0° over 1 hour, and 1.0 mL (0.016 mol) of iodomethane was added. The reaction mixture was stored at 25° for 3 days, then poured into saturated aqueous NH4Cl. The aqueous layer was extracted twice with ether, and the combined organic layers were dried (MgSO4) and evaporated to give 5.2 g of the title compound as a yellow oil: nD 1.5694; ir (neat) 1710 (w), 1663; nmr (CDCl3) δ 0.7 (3H, s), 2.3 (3H, s), 4.6 (2H, s), 7.0 (4H, m), 7.4 (4H, m), 7.8 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04729986
출처 데이터셋uspto-grants-1988_03
ORD IDord-51ec5a26e53c466f9b23a21e9f5dcf19
출처 메모uspto-grants-1988_03