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HRID 390649作成日:2026年10月27日

Trimethyl borate → [3-(Methylamino)phenyl]boronic acid

https://huagongshe.com/reaction/390649

反応式

関与物質

役割名称HCID仕込み量
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Diethyl EtherHCID 3283—
溶媒PentaneHCID 8003—
溶媒TetrahydrofuranHCID 8028—
生成物[3-(Methylamino)phenyl]boronic acidHCID 2355898040%

反応条件

温度-78 °C

反応手順

161 mL (242 mmol) of 1.5M methyllithium in diethyl ether are added dropwise to a solution precooled to −78° C. of 37.6 g (202 mmol) of (3-bromophenyl)methylamine (prepared according to Example 24f) in 300 mL of tetrahydrofuran. After stirring for 1 hour at −78° C., 261 mL (444 mmol) of a 1.7M solution of tert-butyllithium in pentane are added dropwise and the medium is again stirred at −78° C. for 1 hour. At −65° C., 103.5 mL (808 mmol) of trimethyl borate are added dropwise and the reaction medium is then stirred, while allowing the temperature to rise to room temperature over 1 hour. After addition of ice, the reaction medium is extracted with a 1/1 heptane/ethyl acetate mixture and then with 1-butanol. The organic phases are combined, washed with water, dried over magnesium sulfate, filtered and evaporated; 11 g (40%) of 3-methylaminophenylboronic acid are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383652B2
出典データセットuspto-grants-2013_02
ORD IDord-b428150b7c4f48f1a717c700223a4d6d
出典メモuspto-grants-2013_02