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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Benzyl piperazine-1-carboxylate | HCID 643495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl 4-(2-methoxy-2-oxoethyl)piperazine-1-carboxylate | HCID 66728950 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115127B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-767db109e6f4462cbca2356375895b2b |
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| Source note | uspto-grants-2015_08 |
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