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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518714Generated: November 2, 2026

Methyl bromoacetate → benzyl 4-(2-methoxy-2-oxoethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/518714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
SolventTetrahydrofuranHCID 8028—
Productbenzyl 4-(2-methoxy-2-oxoethyl)piperazine-1-carboxylateHCID 6672895092%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of benzyl piperazine-1-carboxylate (0.5 g, 2.270 mmol) and TEA (0.949 mL, 6.81 mmol) in THF (10 mL) was added methyl 2-bromoacetate (0.230 mL, 2.497 mmol) dropwise. The reaction was stirred at 65° C. After 1 hour, the reaction mixture was concentrated, and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated to generate benzyl 4-(2-methoxy-2-oxoethyl)piperazine-1-carboxylate as a clear oil (0.61 g, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-767db109e6f4462cbca2356375895b2b
Source noteuspto-grants-2015_08