Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl iodide → bis(4-Fluorophenyl)methyl(5-methylthiocarbonyl-1H-1,2,4-triazol-1-ylmethyl)silane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Carbonyl Sulfide | HCID 10039 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Flusilazole | HCID 73675 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | bis(4-Fluorophenyl)methyl(5-methylthiocarbonyl-1H-1,2,4-triazol-1-ylmethyl)silane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04729986 |
| 출처 데이터셋 | uspto-grants-1988_03 |
| ORD ID | ord-51ec5a26e53c466f9b23a21e9f5dcf19 |
| 출처 메모 | uspto-grants-1988_03 |