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HRID 18409作成日:2026年10月24日

Bromoacetic Acid → 2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide

https://huagongshe.com/ja/reaction/18409

反応式

関与物質

役割名称HCID仕込み量
反応物Bromoacetic AcidHCID 6227—
反応物4-MethylmorpholineHCID 7972—
反応物Isobutyl chloroformateHCID 62365—
反応物Sodium BicarbonateHCID 516892—
反応物2-(1Adamantyl)-n-pentylethylamine hydrochlorideHCID 49831680—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamideHCID 57479899—

反応条件

温度-15 °C

反応手順

Bromoacetic acid (0.50 g, 3.6 mmol) was dissolved in anhydrous tetrahydrofuran (20 ml), and the solution was stirred at −15° C. under a nitrogen atmosphere. N-Methylmorpholine (0.40 ml, 3.6 mmol) and isobutyl chlorocarbonate (0.45 ml, 3.5 mmol) were added to the solution. Then a solution of a free base of 2-(1-adamantyl)-N-pentylethylamine hydrochloride (Intermediate No. 1-1, 1.0 g, 3.5 mmol) in anhydrous tetrahydrofuran (20 ml) was added dropwise to the mixture. The whole was stirred at 0° C. for 1.5 hours, then a saturated aqueous sodium hydrogencarbonate solution (70 ml) and ethyl acetate (70 ml) were added to the reaction mixture to distribute it. The ethyl acetate layer was washed with water (70 ml) and a saturated aqueous sodium chloride solution (70 ml) successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide (1.3 g, quantitatively) as an oily matter.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741346B2
出典データセットuspto-grants-2010_06
ORD IDord-e19bd88eb6a84b79b364774825249667
出典メモuspto-grants-2010_06