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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 928933생성일: 2026년 10월 26일

Carbon Dioxide → 5-Benzoxy-2,3,4-trifluorobenzoic acid

https://huagongshe.com/reaction/928933

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물SulfolaneHCID 31347—
반응물Lithium diisopropylamideHCID 2724682—
반응물1-(Benzyloxy)-2,3,4-trifluorobenzeneHCID 83396906—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
용매1,4-DioxaneHCID 31275—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물5-Benzoxy-2,3,4-trifluorobenzoic acidHCID 89704915—

반응 단계

To a solution of 1-benzyloxy-2,3,4-trifluorobenzene in appropriate inert solvent (such as, but not limited to, aliphatic and aromatic hydrocarbon (such as pentane, hexane, heptane, cyclohexane, petroleum ether, petrol, gasoline, benzene, toluene, xylene), ether (such as diethyl ether, dibutyl ether, glycol dimethyl ether, 2-methoxyethyl ether, tetrahydrofuran, dioxane), sulfolane, HMPA, DMPU, prefer anhydrous THF, ethyl ether and dioxane) was added strong base (such as LDA, n-BuLi, LiHDMS) at low temperature (−50-−80° C., prefer −78° C.) under nitrogen atmosphere. The stirring was maintained at this temperature for several hours (such as 0.5-12 h, prefer 0.5-2 h). The mixture was transferred to a bottle with dry ice. The mixture is stirred for some time (such as 3-12 h, prefer 5-10 h). 5-Benzoxy-2,3,4-trifluorobenzoic acid is obtained after conventional workup.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290468B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-f8dd96d010bb4bc1b057b85424419897
출처 메모uspto-grants-2016_03