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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250853생성일: 2026년 10월 27일

Hydrochloric Acid → [3-(Methylamino)phenyl]boronic acid

https://huagongshe.com/reaction/250853

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Trimethyl borateHCID 8470—
반응물3-Bromo-N-methylanilineHCID 7018299—
반응물HCID 178418306HCID 178418306—
반응물HCID 178418348HCID 178418348—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물[3-(Methylamino)phenyl]boronic acidHCID 2355898014%

반응 조건

온도-70 °C

반응 단계

166 mL (0.242 mol, 1.2 eq) of 1.6 M methyllithium in diethyl ether are added to a solution cooled to −70° C. of 37.6 g (0.202 mol, 1 eq) of 3-bromo-N-methylaniline (prepared in Example 7c) in 300 ml of tetrahydrofuran. The reaction medium is stirred at −70° C. for one hour and 306 mL (0.444 mol, 2.2 eq) of 1.5 M tert-butyllithium in diethyl ether are then added. The reaction medium is stirred at −70° C. for 45 minutes and 103.5 mL (0.808 mol, 4 eq) of trimethyl borate are then added. The reaction medium is stirred at room temperature for one hour and then hydrolyzed by addition of ice, acidified with 1 L of 2N hydrochloric acid and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over magnesium sulfate. The solvent is evaporated off and 4.2 g (14%) of 3-(methylamino)phenylboronic acid are obtained. The aqueous phase is basified and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over magnesium sulfate. The solvent is evaporated off and the residue is chromatographed on silica gel (8/2 heptane/ethyl acetate). 3.4 g (11%) of 3-(methylamino)phenylboronic acid are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863332B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-20e8989d805a49b59bfede49341709c5
출처 메모uspto-grants-2011_01