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HRID 216177作成日:2026年10月26日

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

https://huagongshe.com/reaction/216177

反応式

関与物質

役割名称HCID仕込み量
反応物Tributyl borateHCID 12712—
反応物2-(3-Bromophenyl)propanoic acidHCID 12797954—
反応物HCID 178418306HCID 178418306—
溶媒Diethyl EtherHCID 3283—
生成物3-(1-Carboxy-ethyl)-phenyl boronic acidHCID 57636070—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193183B2
出典データセットuspto-grants-2012_06
ORD IDord-33babe47ffbc4957a900b1aba4e92a00
出典メモuspto-grants-2012_06