Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402736Generated: October 28, 2026

Chloroacetyl chloride → Isopropyl 2-(morpholinoamino)-4-oxo-4,5-dihydrofuran-3-carboxylate

https://huagongshe.com/reaction/402736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantN-AminomorpholineHCID 20315—
ReactantDiisopropyl malonateHCID 83223—
ReactantIsopropyl 2-isopropoxy-4-oxo-4,5-dihydrofuran-3-carboxylateHCID 51050080—
SolventEthanolHCID 702—
ProductIsopropyl 2-(morpholinoamino)-4-oxo-4,5-dihydrofuran-3-carboxylateHCID 86708411—

Reaction Steps

To a solution of isopropyl 2-isopropoxy-4-oxo-4,5-dihydrofuran-3-carboxylate (12.2 g, 53.6 mmol), which similarly prepared according to the procedure described in the Example 74, Third step using diisopropyl malonate and chloroacetyl chloride, in ethanol (45 mL), 4-aminomorpholine (5.7 mL, 59.2 mmol) was added at ambient temperature. The mixture was stirred for 18 h. The solvent was removed under reduced pressure, and the crude product was suspended in methyl tert-butyl ether, then the precipitate was collected by filtration, washed with methyl tert-butyl ether and hexane then dried to afford isopropyl 2-(morpholinoamino)-4-oxo-4,5-dihydrofuran-3-carboxylate as solid (11.2 g, y. 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-9401091bbd5f4cd7bb2ee7a7c88ee7d2
Source noteuspto-grants-2014_06