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HRID 1865162作成日:2026年10月27日

Triisopropyl borate → [4-(1,3,4-oxadiazol-2-yl)phenyl]boronic Acid

https://huagongshe.com/reaction/1865162

反応式

関与物質

役割名称HCID仕込み量
反応物Triisopropyl borateHCID 21531—
反応物2-(4-Bromophenyl)-1,3,4-oxadiazoleHCID 715120—
反応物ButyllithiumHCID 178418339—
反応物HCID 178418348HCID 178418348—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物[4-(1,3,4-oxadiazol-2-yl)phenyl]boronic AcidHCID 1021975182%

反応条件

温度-65 °C

反応手順

A solution of methyllithium (8% w/w in diethoxymethane) (65 ml) was added to a suspension of 2-(4-bromophenyl)-1,3,4-oxadiazole (40 g) in tetrahydrofuran (THF) (415 ml) at −65° C. After an hour a solution of n-butyllithium (2.5M in hexanes) (78 ml) was then added at −65° C. After an hour, triisopropylborate (90 ml)) was then added maintaining the reaction mixture at −65° C. The reaction mixture was held at −65° C. for an hour and then warmed to −20° C. and drowned out into a mixture of acetic acid (28 ml) in water (222 ml). The resultant solid was isolated, washed with THF and water, and dried to yield the title compound (28.96 g@ 95.1% w/w, 82%); 400 MHz NMR Spectrum: (DMSOd6) 8.00 (s, 4H), 8.31 (s, 2H), 9.35 (s, 1H); Mass Spectrum MH+ 191.0628 (calc. using 11-B) Found 191.0633.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07626020B2
出典データセットuspto-grants-2009_12
ORD IDord-9cfc45d53b9f4b5e9370cef76535023a
出典メモuspto-grants-2009_12