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HRID 1894812作成日:2026年10月27日

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

https://huagongshe.com/reaction/1894812

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Trimethyl borateHCID 8470—
反応物Benzenemethanamine, 3-bromo-HCID 457587—
反応物HCID 178418306HCID 178418306—
反応物HCID 178418348HCID 178418348—
溶媒TetrahydrofuranHCID 8028—
生成物[3-(Methylamino)phenyl]boronic acidHCID 2355898040%

反応条件

温度-70 °C

反応手順

37.6 g (202 mmol, 1 eq) of (3-bromophenyl)methylamine (obtained as in 1c) are dissolved in 300 mL of tetrahydrofuran. The reaction mixture is cooled to −70° C. and 166 mL (242 mmol, 1.2 eq) of 1.5 M methyllithium are then added slowly, while keeping the temperature at −70° C. The reaction mixture is stirred for 1 hour at −70° C. 306 mL (444 mmol, 2.2 eq) of 1.46 M tert-butyllithium are added, while keeping the temperature at −70° C. The reaction mixture is stirred for 45 minutes at −70° C. 103.5 ml (808 mmol, 4 eq) of trimethyl borate are added at −65° C. and the reaction mixture is then warmed to room temperature. The reaction is stopped by adding 1 L of 1N hydrochloric acid. The pH is adjusted to pH 5 and the reaction medium is then extracted with n-butanol. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 11.3 g of N-methyl-3-aminophenylboronic acid are obtained. Yield=40%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08513297B2
出典データセットuspto-grants-2013_08
ORD IDord-05c0e531d764456687fcb74ed69f2aa9
出典メモuspto-grants-2013_08