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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1386872생성일: 2026년 10월 26일

Hydrochloric Acid → N-(3,4-dihydroxyphenethyl)-2-(3,4-dihydroxyphenyl)-2-hydroxyacetamide

https://huagongshe.com/reaction/1386872

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Dopamine HydrochlorideHCID 65340—
반응물N-HydroxysuccinimideHCID 80170—
반응물(+-)-3,4-Dihydroxymandelic acidHCID 85782—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물N-(3,4-dihydroxyphenethyl)-2-(3,4-dihydroxyphenyl)-2-hydroxyacetamideHCID 9797093—

반응 단계

2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid (300 mg, 1.63 mmol) and N-hydroxysuccinimide (188 mg, 1.63 mmol) were dissolved in 1,4-dioxane (20 ml) under nitrogen, and N,N′-dicyclohexylcarbodiimide (336 mg, 1.63 mmol) was added to the mixture at room temperature, which was stirred at this temperature for 16 h. The by-product which precipitated out was filtered off, and the filtrate was added to a solution of 2-(3,4-dihydroxyphenyl)ethylamine hydrochloride (309 mg, 1.63 mmol) in water (20 ml). Sodium hydrogencarbonate (151 mg, 1.8 mmol) was also added, and the reaction mixture was stirred under nitrogen at 50° C. for 1.5 h. The mixture was rendered acidic using 5% strength hydrochloric acid and extracted 3 times with ethyl acetate (a total of 90 ml). The organic phase was washed with saturated NaCl solution, dried over Na2SO4 and filtered, and the filtrate was evaporated under reduced pressure. The product was purified by chromatography on silica gel using the eluent ethyl acetate. The yield was 266 mg of a colorless syrup (51% of theory based on the acid used).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06265611B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-752eb719072e47dc8f7bd6dcb8c146fd
출처 메모uspto-grants-2001_07