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HRID 1094800作成日:2026年10月27日

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

https://huagongshe.com/reaction/1094800

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylenediaminetetraacetic AcidHCID 6049—
反応物CyclohexaneHCID 8078—
反応物1-Chloro-4-(trifluoromethoxy)benzeneHCID 2777273—
反応物FluorodimethoxyboraneHCID 3083563—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Chloro-2-(trifluoromethoxy)phenyl)boronic acidHCID 53216719—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08134007B2
出典データセットuspto-grants-2012_03
ORD IDord-0d1e6e05ceb246bfac11c2f48e955d55
出典メモuspto-grants-2012_03