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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421206Generated: October 26, 2026

Ethyl Acetate → Diethyl 1-(bromoacetyl)-2,2-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/421206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetyl bromideHCID 61147—
ReactantDiethyl 2,2-pyrrolidinedicarboxylateHCID 12524347—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductDiethyl 1-(bromoacetyl)-2,2-pyrrolidinedicarboxylateHCID 59215802—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diethyl 2,2-pyrrolidinedicarboxylate (D63, 900 mg) in dichloromethane (9 mL) at 0° C., potassium carbonate (0.5M solution, 12.5 mL) and bromoacetyl bromide (0.55 mL) were added. The resulting mixture was stirred at 0° C. for 2 hours. The mixture was then diluted with water and then allowed to reach r.t. Ethyl acetate (15 mL) was added and phases were separated. The aqueous phase was then extracted with ethyl acetate (2×10 mL) and washed with brine (20 mL). The organic phase was dried and concentrated in vacuo to give the desired compound (1.06 g) as orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097618B2
Source datasetuspto-grants-2012_01
ORD IDord-18773e2065f3476d8a70f05a272ab7d8
Source noteuspto-grants-2012_01