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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
SolventAcetoneHCID 180—
ProductEthyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylateHCID 441864037.8%

Reaction Conditions

Temperature56 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175320B2
Source datasetuspto-grants-2015_11
ORD IDord-def7eb915c75402aae75a597b6533efb
Source noteuspto-grants-2015_11