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HRID 2185939作成日:2026年10月24日

Trimethyl borate → 2-Dimethylamino-6-methoxyphenylboronic acid

https://huagongshe.com/ja/reaction/2185939

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3-Methoxy-N,N-dimethylbenzenamineHCID 139977—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-Dimethylamino-6-methoxyphenylboronic acidHCID 4374258—

反応手順

To a solution of 5.3 g (35 mmol) of 3-dimethylamino-anisole in 25 mL of dry THF at −78° C. was added 19 mL (47 mmol) of a 2.5M solution of n-butyl lithium in hexanes. The reaction mixture was stirred for 1 hour before removing the ice bath and warming to room temperature for 90 minutes. The solution was cooled to −78° C., treated with 8.75 g (84 mmol) of trimethyl orthoborate, and then stirred for one hour before warming to room temperature for one hour. The reaction was quenched by the addition of 20 mL of water and sufficient acetic acid to neutralize the mixture. The reaction mixture was extracted with ethyl acetate (3×30 mL), and the combined organic extracts were extracted with 1N NaOH solution (4×15 mL). The combined aqueous extracts were acidified with acetic acid and extracted with EtOAc (3×20 mL). The organic phase was washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to give 2-methoxy-6-dimethylamino-phenylboronic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06403584B1
出典データセットuspto-grants-2002_06
ORD IDord-6d6ba40121be444d8ee27cbbcb92c9ad
出典メモuspto-grants-2002_06