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HRID 216177생성일: 2026년 10월 26일

Tributyl borate → 3-(1-Carboxy-ethyl)-phenyl boronic acid

https://huagongshe.com/reaction/216177

반응식

참여 물질

역할이름HCID투입량
반응물Tributyl borateHCID 12712—
반응물2-(3-Bromophenyl)propanoic acidHCID 12797954—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
생성물3-(1-Carboxy-ethyl)-phenyl boronic acidHCID 57636070—

반응 단계

A solution of 2-(3-bromo-phenyl)-propionic acid [500 mg, 2.18 mmol, Intermediate (69)] in anhydrous ether (20 mL) is added tert-butyl lithium (1.7 M in pentane, 5.4 mL, 9.16 mmol) dropwise at −78° C. and this mixture is stirred for 30 minutes treated with tributyl borate (2.34 mL, 8.72 mmol). The reaction mixture is allowed to warm up to room temperature, stirred for 15 hours, diluted with ether, and quenched with 1 M H3PO4. After stirring for 30 minutes the ether layer is separated and extracted three times with 2 N sodium hydroxide (20 mL). The combined sodium hydroxide extracts are acidified with 6 N hydrochloric acid to pH=1 and extracted three times with ether (50 mL). The combined organic extracts are washed with brine, dried over sodium sulfate and concentrated to obtain 3-(1-carboxy-ethyl)-phenyl boronic acid [Intermediate (70)] as a solid, which is used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193183B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-33babe47ffbc4957a900b1aba4e92a00
출처 메모uspto-grants-2012_06