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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1007233생성일: 2026년 10월 24일

Dilithium Sulfide → Methyl 2-(difluoromethyl)-4-isobutyl-5-mercapto-6-(trifluoromethyl)-3-pyridinecarboxylate

https://huagongshe.com/ko/reaction/1007233

반응식

참여 물질

역할이름HCID투입량
반응물Dilithium SulfideHCID 10290727—
반응물Methyl 5-bromo-2-(difluoromethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylateHCID 15117750—
용매Hydrochloric AcidHCID 313—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(difluoromethyl)-4-isobutyl-5-mercapto-6-(trifluoromethyl)-3-pyridinecarboxylateHCID 997471183%

반응 단계

To a stirred solution of 10.11 g (0.026 mol) of methyl 5-bromo-2-(difluoromethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate (example 122 of U.S. Pat. No. 5,019,153) in 75 mL dry DMF was added 1.42 g (0.031 mol) of lithium sulfide in one portion and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with 150 mL of 10% HCl solution and extracted with ether (3×100 mL). The combined extracts were washed with water, dried (MgSO4) and evaporated. The residue was purified by kugelrohr distillation (oven temperature 100-110° C., 1.5 torr) to give 7.35 g (83%) of product as a yellow-green oil:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06794396B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-766168fc4bfb48ec9b97ac4cb6d51185
출처 메모uspto-grants-2004_09