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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094800생성일: 2026년 10월 27일

Ethylenediaminetetraacetic Acid → (5-Chloro-2-(trifluoromethoxy)phenyl)boronic acid

https://huagongshe.com/reaction/1094800

반응식

참여 물질

역할이름HCID투입량
반응물Ethylenediaminetetraacetic AcidHCID 6049—
반응물CyclohexaneHCID 8078—
반응물1-Chloro-4-(trifluoromethoxy)benzeneHCID 2777273—
반응물FluorodimethoxyboraneHCID 3083563—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
생성물(5-Chloro-2-(trifluoromethoxy)phenyl)boronic acidHCID 53216719—

반응 단계

To a solution of the 4-chloro(trifluoromethoxy)benzene (2.0 g, 10.18 mmol) in dry tetrahydrofuran (THF, 30 ml) at −78° C., was added ethylenediaminetetraacetic acid (EDTA, 1.24 g, 10.7 mmol) followed by a 1.3 M solution of sec-butyllithium in cyclohexane (7.63 ml, 10.7 mmol) and the reaction stirred for 2 hours under nitrogen. To this reaction mixture at −78° C., was then added dropwise the preformed dimethoxyfluoroborane mixture. The reaction was stirred at −78° C. for 30 minutes, warmed to room temperature for 30 minutes, and then quenched with water (10 ml). The reaction mixture was extracted with diethyl ether (4×50 ml). The combined organic extracts were dried over MgSO4 and concentrated in vacuo. To purify, the residue was dissolved in diethyl ether (10 ml) and washed with an aqueous solution of 10% NaOH (50 ml). The aqueous layer was acidified and extracted with ethyl acetate (3×40 ml). The combined ethyl acetate extracts were dried over MgSO4 and concentrated in vacuo to afford a mixture of the title compound and its corresponding regioisomer as a white solid (0.862 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08134007B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-0d1e6e05ceb246bfac11c2f48e955d55
출처 메모uspto-grants-2012_03