HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707768Generated: October 25, 2026
Ethyl bromoacetate → Ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylate
https://huagongshe.com/reaction/707768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-oxocyclopentanecarboxylate | HCID 69136 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylate | HCID 4418640 | 37.8% |
Reaction Steps
To a solution of ethyl 2-oxocyclopentanecarboxylate (93.27 g, 597 mmol) and ethyl 2-bromoacetate (144.64 g, 866 mmol) in acetone (1.2 L) was added K2CO3 (165 g, 1194 mmol). The mixture was heated at 56° C. for 24 h. The solid was filtered off and the filter cake was washed with acetone (3×100 mL). The filtrate was concentrated and the resultant liquid was purified by a silica gel plug to give the title compound as light yellow liquid (54.7 g). LCMS m/z=243.3 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 1.23 (t, J=7.14 Hz, 3H), 1.24 (t, J=7.14 Hz, 3H), 1.95-2.03 (m, 1H), 2.06-2.15 (m, 2H), 2.35-2.50 (m, 2H), 2.55-2.60 (m, 1H), 2.80 (dd, J=15.2, 2.09 Hz, 1H), 2.95 (dd, J=15.2, 2.09 Hz, 1H), 4.09 (q, J=7.14 Hz, 2H), 4.12 (q, J=7.14 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09175320B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-def7eb915c75402aae75a597b6533efb |
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| Source note | uspto-grants-2015_11 |
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