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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250909생성일: 2026년 10월 27일

Trimethyl borate → 3-(1-Methyl-3-pentylureido)phenylboronic acid

https://huagongshe.com/reaction/250909

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl borateHCID 8470—
반응물1-(3-Bromophenyl)-1-methyl-3-pentylureaHCID 67272794—
반응물HCID 178418306HCID 178418306—
반응물HCID 178418348HCID 178418348—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물3-(1-Methyl-3-pentylureido)phenylboronic acidHCID 6727327239%

반응 단계

In a manner similar to that of Example (18a), by reaction of 123 g (0.411 mol, 1 eq) of 1-(3-bromophenyl)-1-methyl-3-pentylurea in 1.23 L of tetrahydrofuran, 150 mL (0.452 mol, 1.1 eq) of methyllithium, 530 mL (0.904 mol, 2.2 eq) of a 1.7 M solution of tert-butyllithium in pentane and 115 mL (0.904 mol, 2.2 eq) of trimethyl borate, and after purification by chromatography on silica gel (50/50 heptane/ethyl acetate) and crystallization from ethyl acetate/heptane, 42.0 g of 3-(1-methyl-3-pentylureido)phenylboronic acid are obtained in the form of a pink-colored powder. Yield=39%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863332B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-b51e54c96bc14c959fc6dba60834ce53
출처 메모uspto-grants-2011_01