HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074853Generated: October 26, 2026
Ethyl Acetate → Diethyl 1-(bromoacetyl)-2,2-pyrrolidinedicarboxylate
https://huagongshe.com/reaction/2074853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Diethyl 2,2-pyrrolidinedicarboxylate | HCID 12524347 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diethyl 1-(bromoacetyl)-2,2-pyrrolidinedicarboxylate | HCID 59215802 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919491B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-dfe98758f79d45268047e7f689880e97 |
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| Source note | uspto-grants-2011_04 |
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