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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 973524Erstellt: 25. Oktober 2026

4-Methylmorpholine → Benzyl (tert-butoxycarbonyl)glycylglycinate

https://huagongshe.com/reaction/973524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
EduktN-(tert-butoxycarbonyl)glycineHCID 78288—
Eduktp-ToluenesulfonateHCID 85570—
EduktBenzyl glycinateHCID 409140—
LösungsmittelChloroformHCID 6212—
LösungsmittelAcetonitrileHCID 6342—
ProduktBenzyl (tert-butoxycarbonyl)glycylglycinateHCID 324452493,7%

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

Boc-Gly-OH (17.52 g, 0.1 mole) in a mixture of CHCl3 (50 ml) and acetonitrile (50 ml) was cooled to -15° C. and EDCI (19.17 g, 0.1 mole) was added and stirred for 20 minutes. To this, a pre-cooled solution of H-Gly-OBzl.tosylate (37.1 g, 0.11 mole), NMM (12.09 ml, 0.11 mole) in CHCl3 (100 ml) was added and stirred overnight at room temperature. After removing the solvent, the residue was taken in CHCl3 and extracted with acid and base. Chloroform was removed under reduced pressure, triturated with pet. obtain 30.2 g of I (yield: 93.7%), m.p. 82°-83° C. Rf2, 0.52; Rf4, 0.82. Anal. Cald. for C16H22N2O5 : C, 59.61; H, 6.88, N, 8.69%. Found: C, 59.43; H, 6.88; N, 8.35%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05064430
Quelldatensatzuspto-grants-1991_11
ORD IDord-f8fa9cbcb0a64d688ab524bf26179d5f
Quellennotizuspto-grants-1991_11