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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086785Generated: October 26, 2026

4-Methylmorpholine → Benzyl (tert-butoxycarbonyl)glycylglycinate

https://huagongshe.com/reaction/1086785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
Reactantp-ToluenesulfonateHCID 85570—
ReactantBenzyl glycinateHCID 409140—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductBenzyl (tert-butoxycarbonyl)glycylglycinateHCID 324452493.7%

Reaction Conditions

Temperature-15 °C

Reaction Steps

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. ether, filtered, washed with pet. ether and dried to obtain 30.2 g of I (yield: 93.7%), m.p. 82°-83° C. Rf2, 0.52; Rf4, 0.82. Anal. Calcd. for C16H22N2O5 : C, 59.61; H, 6.88; N, 8.69%. Found C, 59.43; H, 6.88; N, 8.35%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032271
Source datasetuspto-grants-1991_07
ORD IDord-f3d2146e602044d387d3409607c9d625
Source noteuspto-grants-1991_07