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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366410Generated: October 29, 2026

1,2-Dichloroethane → (3R)-5-oxo-N,4-bis(phenylmethyl)-3-morpholinecarboxamide

https://huagongshe.com/reaction/1366410

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzylamineHCID 7504—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(R)-4-Benzyl-5-oxo-3-morpholinecarboxylic AcidHCID 13543371—
SolventDichloromethaneHCID 6344—
Product(3R)-5-oxo-N,4-bis(phenylmethyl)-3-morpholinecarboxamideHCID 59452664101%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (3R)-5-oxo-4-(phenylmethyl)-3-morpholinecarboxylic acid (69.67 g, 296.2 mmol) and 1-hydroxybenzotriazole (48.01 g, 355.4 mmol) in DCM (990 mL) was cooled to 0° C. To the mixture was added 4-methylmorpholine (163 mL, 1483 mmol), benzyl amine (35.6 mL, 325.9 mmol), and EDC (62.46 g, 325.8 mmol). The yellow solution was stirred overnight at room temperature, and was then washed with water (500 mL), 6 N aqueous HCl (300 mL), and water (200 mL). The organic phase was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give crude (3R)-5-oxo-N,4-bis(phenylmethyl)-3-morpholinecarboxamide (97.05 g, >100% crude yield) as a yellow foam. LCMS: (M+H)+: 325.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-74197559e0454736b72b60b8f09ad410
Source noteuspto-grants-2011_02