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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1178557Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1178557

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium cyanoborohydrideHCID 5003444—
EduktDi-tert-butyl (R)-2-aminopentanedioateHCID 7019734—
EduktMethyl 4-(2-oxoethyl)benzoateHCID 13844675—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 1-{2-[4-(methoxycarbonyl)phenyl]ethyl}-5-oxo-d-prolinateHCID 6925087675%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07276531B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-cf0abaa5498f49baa16edd46e0e63997
Quellennotizuspto-grants-2007_10