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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884264생성일: 2026년 10월 26일

Hydrochloric Acid → N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-3-hydroxy-2-(4-methylphenyl)acrylamide

https://huagongshe.com/reaction/1884264

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물tert-Butoxy bis(dimethylamino)methaneHCID 79885—
반응물N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamideHCID 23509014—
용매TetrahydrofuranHCID 8028—
생성물N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-3-hydroxy-2-(4-methylphenyl)acrylamideHCID 6990048474%

반응 조건

온도80 °C

반응 단계

2.40 g (5.95 mmol) of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide and 3.10 g (17.8 mmol) of t-butoxybis(dimethylamino) methane were mixed and stirred at 80° C. for 2 hours. The reaction mixture was cooled and tetrahydrofuran was added thereto. The reaction mixture was acidified with hydrochloric acid and stirred at room temperature for 2 hours. After the solvent was distilled off under reduced pressure, the residue was extracted with chloroform washed with saturated brine twice, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel chromatography (eluent, hexane:ethyl acetate=3:2) and dried to give 1.90 g of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-3-hydroxy-2-(4-methylphenyl)acrylamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06762321B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-3d3def96f8e04ab6ad88fa043a553c78
출처 메모uspto-grants-2004_07