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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234757생성일: 2026년 10월 25일

4-Bromo-2-fluorotoluene → 4,5-Dihydro-5,5-dimethyl-2-(3'-fluoro-4'-methyl-biphenyl-2-yl)oxazole

https://huagongshe.com/reaction/234757

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromo-2-fluorotolueneHCID 171040—
반응물MagnesiumHCID 5462224—
반응물4,5-Dihydro-5,5-dimethyl-2-(2-methoxyphenyl)-oxazoleHCID 54275939—
용매TetrahydrofuranHCID 8028—
생성물4,5-Dihydro-5,5-dimethyl-2-(3'-fluoro-4'-methyl-biphenyl-2-yl)oxazoleHCID 54515599—

반응 단계

14.7 g (605.7 mol) of magnesium filings are initially introduced into 50 ml of analytical grade tetrahydrofuran under argon, and 117.7 g (623 mmol) of 4-bromo-2-fluorotoluene in 500 ml of analytical grade tetrahydrofuran are added, while stirring. A clear solution forms at 35°-40° C. within 2 hours. A solution of 74.0 g (360.5 mmol) of the compound from Example II in 500 ml of analytical grade tetrahydrofuran is added dropwise at room temperature and the mixture is subsequently stirred at about 25° C. for 16 hours, initially with gentle cooling. The solvent is evaporated off and the crude product is subsequently rinsed in 600 ml of ethyl acetate and 800 ml of saturated ammonium chloride solution at 10° C., dried with sodium sulphate and evaporated in vacuo. For purification, the product is taken up in 600 ml of ether, any solid residue is filtered off with suction and the crude product is extracted into the aqueous phase by several extractions with 2M hydrochloric acid. This aqueous phase is covered with a layer of ether and brought to pH 13 with sodium hydroxide solution. After three extractions with ether, the product phase is dried with sodium sulphate and evaporated and the residual solvent is removed under a high vacuum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596006
출처 데이터셋uspto-grants-1997_01
ORD IDord-4c08463fbfa14a9a93d05e0673945953
출처 메모uspto-grants-1997_01