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HRID 41781作成日:2026年10月25日

Hydrochloric Acid → 4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride)

https://huagongshe.com/reaction/41781

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4-BromotriphenylamineHCID 642838—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride)HCID 1216693459.9%

反応条件

温度-80 °C

反応手順

10 g (30 mmol) of 4-bromotriphenylamine was put into a 500 mL three-neck flask. The air in the flask was replaced with nitrogen. To the mixture were added 20 mL of tetrahydrofuran (THF), and then the mixture was stirred at −80° C. Into this solution, 20 mL (32 mmol) of n-butyllithium (a 1.6 mol/L hexane solution) was dropped by a syringe. After the dropping, this solution was stirred at the same temperature for 1 hour. After the stirring, 40 mL (60 mmol) of trimethyl borate was added to the solution, and the solution was stirred for 1 hour while the temperature of the solution was being increased to room temperature. To the solution was added 200 mL (1.0 mol/L) of hydrochloric acid, and then the solution was stirred for about 15 hours. The organic layer was washed with a saturated sodium hydrogen carbonate solution and then a saturated saline solution. Then, the organic layer was dried with magnesium sulfate. This mixture was subjected to gravity filtration. The obtained filtrate was condensed to give a white solid. The obtained solid was recrystallized with chloroform/hexane to give 5.2 g of a white powdered solid, which was the object of the synthesis, at a yield of 58%. A synthesis scheme of Step 2 is shown in (c-2) given below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530672B2
出典データセットuspto-grants-2013_09
ORD IDord-637c338567364dec916a49f0d7552336
出典メモuspto-grants-2013_09