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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178557생성일: 2026년 10월 27일

Acetic Acid → Tert-butyl 1-{2-[4-(methoxycarbonyl)phenyl]ethyl}-5-oxo-d-prolinate

https://huagongshe.com/reaction/1178557

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Di-tert-butyl (R)-2-aminopentanedioateHCID 7019734—
반응물Methyl 4-(2-oxoethyl)benzoateHCID 13844675—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 1-{2-[4-(methoxycarbonyl)phenyl]ethyl}-5-oxo-d-prolinateHCID 6925087675%

반응 단계

To a solution of H-D-Glu(OtBu)-OtBu, commercially available from Bache (0.5 g, 2.23 mmol) in MeOH (15 mL) were added 4-carbomethoxyphenylacetaldehyde (obtained from methyl 4-formyl benzoate as described in Nair et al., 1989) (0.4 g, 2.23 mmol), acetic acid (0.15 mL, 2.67 mmol), and NaCNBH3 (3.3 mL, 1.0 M THF solution, 3.3 mmol). The resulting solution was stirred at RT for 3 h then was diluted with EtOAc (100 mL) and washed with water (50 mL), and brine (50 mL). The organic solution was dried over sodium sulfate and concentrated in vacuo. The crude oil was diluted with xylene and the solution refluxed for 5 h. This solution was concentrated under reduced pressure and purified by silica gel column chromatography using EtOAc/hexane as eluent to afford the title compound (0.75 g, 75%) as a white solid. Rj 0.45 (EtOAc/hexane 1/1); 1H NMR (CDCl3) δ 1.47 (s, 9H), 1.95-2.05 (m, 1H), 2.10-2.20 (m, 1H), 2.25-2.35 (m, 1H), 2.40-2.50 (m, 1H), 2.80-3.00 (m, 2H), 3.10-3.20 (m, 1H), 3.82 (dd, 1H), 3.91 (s, 3H), 3.90-4.01 (m, 1H), 7.25 (d, 2H), 7.96 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276531B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-cf0abaa5498f49baa16edd46e0e63997
출처 메모uspto-grants-2007_10