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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234711생성일: 2026년 10월 25일

1,2-Dichlorobenzene → 2-Bromo-5-(4-fluorophenyl)-4-[4-(methylsulfonyl)phenyl]-6-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/234711

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichlorobenzeneHCID 7239—
반응물Phosphorus pentabromideHCID 62678—
반응물Potassium BromideHCID 253877—
반응물5-(4-Fluorophenyl)-4-[4-(methylsulfonyl)phenyl]-6-(trifluoromethyl)-2-oxo-pyridineHCID 23355258—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-Bromo-5-(4-fluorophenyl)-4-[4-(methylsulfonyl)phenyl]-6-(trifluoromethyl)pyridineHCID 1027709637.2%

반응 단계

A mixture of 0.35 g of 5-(4-fluorophenyl)-4-[4-(methylsulfonyl)phenyl]-6-(trifluoromethyl)-2-oxo-pyridine (step 5 of Example 1), 3 g of phosphorus pentabromide, 0.3 g of potassium bromide and 10 mL of 1,2-dichlorobenzene was held at reflux for 2 hours. The reaction mixture was cooled. An addition 3.7 g of phosphorus pentabromide was added to the reaction mixture and the reaction mixture was held at 90° C. for 8 hours, and at 180°-190° C. for 2 days. The reaction mixture was cooled and stirred with water and methylene chloride. The methylene chloride layer was dried over MgSO4 and filtered through silica gel. The methylene chloride filtrate was concentrated in vacuo and the residue was purified by HPLC (20% ethyl acetate/hexane then 50% ethyl acetate/hexane). The fraction eluted with 50% ethyl acetate/hexane yielded a solid. Recrystallization from methylene chloride/hexane yielded 150 mg of white solid: mp 187.5°-189° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596008
출처 데이터셋uspto-grants-1997_01
ORD IDord-9f4fb3f797e6435ba01617398cd780ee
출처 메모uspto-grants-1997_01