Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889215Generated: November 1, 2026

Potassium Carbonate → Benzyl 2-(2-(methylcarbamoyl)morpholino)acetate

https://huagongshe.com/reaction/889215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl bromoacetateHCID 62576—
ReactantTert-butyl 2-(methylcarbamoyl)morpholine-4-carboxylateHCID 66760938—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-(2-(methylcarbamoyl)morpholino)acetateHCID 66760795—

Reaction Steps

tert-butyl 2-(methylcarbamoyl)morpholine-4-carboxylate prepared above (0.5 g, 0.20 mmol) was dissolved in DCM (10 mL) and TFA (2 mL). The reaction mixture was stirred at room temperature for 4 h and then concentrated; excess 1N HCl solution in ether was added to the residue and concentrated under high vacuum. The residue was dissolved in acetonitrile (20 mL) and K2CO3 (0.56 g, 40.8 mmol) was added followed by bromo-acetic acid benzyl ester (0.7 g, 3.07 mmol). The reaction mixture was heated at 60° C. overnight. The solution was cooled to room temperature and diluted with Ethyl acetate (50 mL) and water (50 mL), organic layer was separated, dried (MgSO4) and concentrated to give an oil which was purified by column chromatography using ethyl acetate-hexanes (1:1) to give benzyl 2-(2-(methylcarbamoyl)morpholino)acetate. MS (APCI) 293 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252793B2
Source datasetuspto-grants-2012_08
ORD IDord-f0ce767ba1e9435bbb4f8676414f6827
Source noteuspto-grants-2012_08