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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381582생성일: 2026년 10월 26일

Glutamic acid diethyl ester hydrochloride → diethyl(S)-2-(4-nitrophthalimido)glutarate

https://huagongshe.com/reaction/381582

반응식

참여 물질

역할이름HCID투입량
반응물Glutamic acid diethyl ester hydrochlorideHCID 73960—
반응물DiisopropylethylamineHCID 81531—
반응물4-Nitrophthalic acid anhydrideHCID 230976—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물diethyl(S)-2-(4-nitrophthalimido)glutarateHCID 10429715—

반응 단계

Diisopropylethylamine (24 ml, 0.138 mole) (Aldrich) was added to a suspension of 4-nitrophthalic anhydride (25 g, 0.13 mole) (Tokyo Kasei) and L-glutamic acid diethyl ester hydrochloride (35 g, 0.146 mole) (Aldrich) in toluene (130 ml). The reaction mixture was stirred at reflux utilizing a Dean-Stark trap for 2.5 hours. After cooling, the solution was diluted with diethyl ether (300 ml), washed with water (75 ml), saturated NaHCO3 solution (50 ml), dried (MgSO4), and concentrated in vacuo at 70° C. to give diethyl(S)-2-(4-nitrophthalimido)glutarate as an oil that solidified to a white solid on standing (35.8 g). M.P.=65.5-66.5° C. 1H NMR (DMSO-d6, 300 MHz) δ: 1.12 (t, J=7 Hz, 3H, ester CH3), 1.14 (t, J=7 Hz, 3H, ester CH3), 2.2-2.5 (m, 4H, glu CH2CH2), 3.96 (q, J=7 Hz, 2H, ester CH2), 4.08-4.19 (m, 2H, ester CH2), 4.97-5.04 (m, 1H, glu CH), 8.19 (dd, J=8,0.5 Hz, 1H, Ar), 8.56 (dd,=2,0.5 Hz, 1H, Ar), 8.68 (dd, J=8,2 Hz, 1H, Ar). Mass spectrum (CI—CH4); 379 (M+1, 28.8%), 333 (71.6%), 305 (100%). Anal. Calculated for C17H18N2O8: C, 53.97; H, 4.80; N, 7.40. Found: C, 53.89; H, 4.82; N, 7.42.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06306865B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-c511e394a895437eac28589c1e4caa66
출처 메모uspto-grants-2001_10