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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11479생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/11479

반응식

참여 물질

역할이름HCID투입량
반응물Bromoacetic AcidHCID 6227—
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물Sodium BicarbonateHCID 516892—
반응물2-(1Adamantyl)-n-pentylethylamine hydrochlorideHCID 49831680—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamideHCID 57479899—

반응 조건

온도-15 °C

반응 단계

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, a saturated aqueous sodium hydrogencarbonate solution (70 ml) and ethyl acetate (70 ml) were added to the reaction mixture, and the reaction mixture was distributed. The ethyl acetate layer was washed with water (70 ml) and a saturated aqueous sodium chloride solution (70 ml) successively and dried over anhydrous magnesium sulfate. The ethyl acetate layer was concentrated under reduced pressure to give 1.3 g (quantitatively) of 2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide as a oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098226B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7be440cf55a742dbbf2f5f861b28233a
출처 메모uspto-grants-2006_08