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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233628생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → Methyl (R)-4-[(2-hydroxy-1-phenylethyl)amino]-4-oxo-2-butenoate

https://huagongshe.com/reaction/233628

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물(R)-beta-aminophenethyl alcoholHCID 2724025—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물(E)-4-methoxy-4-oxobut-2-enoateHCID 21721168—
용매Ethyl AcetateHCID 8857—
생성물Methyl (R)-4-[(2-hydroxy-1-phenylethyl)amino]-4-oxo-2-butenoateHCID 53871317—

반응 단계

To a solution of monomethyl fumarate (3.0 g, 23 mmol) in ethyl acetate (40 mL) was added 1-hydroxybenzotriazole hydrate (3.0 g, 22 mmol), followed by N,N'-dicyclohexylcarbodiimide (4.5 g, 22 mmol) and the reaction stirred at ambient temperature for 1 hour. The solid was filtered off and discarded. To the filtrate was added (R)-α-phenylglycinol (3.0 g, 22 mmol ) and stirring continued for 20 minutes. The volatiles were removed in vacuo (40° C.) and the residue purified by flash chromatography on normal phase silica gel using hexane: ethyl acetate (1:1) as eluant. Recovered 2.5 g (46%) of (18) as a white solid, m.p. 75°-77° C.; IR (neat) 3250 (OH), 1729 (C=O ester), 1666 (C=O amide), 1640 (C=C)cm-1 ;NMR (CDCl3) δ 7.3-7.4 (5H, m, Ph), 7.0 (1H, d, J 15 Hz, trans alkene), 6.8 (1H, d, J 15 Hz, trans alkene), 6.6 (1H, br d, NH), 5.2 (1H, m, CH), 3.9 (2H, t, J 3 Hz, CH2), 3.8 (3H, s, CH3), 2.3 (1H, t, J 5 Hz, OH); [α]D -53° (CHCl3, 24° C., c=1); anal C13H15NO4 ; requires C 62.64% H 6.07% N 5.62%; found C 62.72% H 5.92% N 5.48%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05593967
출처 데이터셋uspto-grants-1997_01
ORD IDord-d97dbee2fa244c0bb9d07ea0152a6b60
출처 메모uspto-grants-1997_01