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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814739Generated: October 29, 2026

1,2-Dichloroethane → tert-Butyl [2-(morpholin-4-yl)-2-oxoethyl]carbamate

https://huagongshe.com/reaction/1814739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantDiisopropylethylamineHCID 81531—
SolventDimethylformamideHCID 6228—
Producttert-Butyl [2-(morpholin-4-yl)-2-oxoethyl]carbamateHCID 1053825955.1%

Reaction Steps

To a stirred solution of N-(tert-butoxycarbonyl)glycine (3.0 g, 17.1 mmol) in DMF (75 mL), N,N-diisopropylethylamine (14.9 mL, 85.5 mmol) was added, followed by EDC (3.6 g, 18.8 mmol) and HOBT (2.5 g, 18.8 mmol) at 0° C., under argon. The resulting mixture was stirred for 0.5 h after which time morpholine (3.0 mL, 34.2 mmol) was introduced in a dropwise manner. Upon complete addition, the reaction was warmed to ambient temperature, stirred overnight and concentrated. The resulting residue was diluted with EtOAc and saturated NaHCO3. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organics were dried (MgSO4), filtered and concentrated to give 2.3 g (55%) of (2-morpholin-4-yl-2-oxo-ethyl)-carbamic acid tert-butyl ester which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878706B1
Source datasetuspto-grants-2005_04
ORD IDord-44f71313330d42eeb557bb4c03afbcc1
Source noteuspto-grants-2005_04