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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62799Generated: October 26, 2026

Ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylate → 2-(2-oxocyclopentyl)acetic Acid

https://huagongshe.com/reaction/62799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylateHCID 4418640—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
Product2-(2-oxocyclopentyl)acetic AcidHCID 356998375.1%

Reaction Steps

A solution of ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylate (50.0 g, 206 mmol) in HOAc (500 mL) and 6 M HCl (250 mL) was heated at 100° C. for 6 h. The solvent was removed under reduced pressure and the residue was partitioned between EtOAc (500 mL) and H2O (200 mL). Aqueous layer was separated and extracted with EtOAc (2×250 mL). The combined organic layers were washed with H2O (300 mL), brine (300 mL), dried over Na2SO4, decanted and concentrated to yield the title compound as a white solid (22 g). 1H NMR (400 MHz, CDCl3) δ ppm 1.59-1.72 (m, 1H), 1.75-1.90 (m, 1H), 2.03-2.10 (m, 1H), 2.20 (dd, J=10.9, 8.9 Hz, 1H), 2.30-2.40 (m, 2H), 2.40-2.50 (m, 2H), 2.80 (dd, J=15.7, 7.2 Hz, 1H), 11.5 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447041B2
Source datasetuspto-grants-2016_09
ORD IDord-4505539facc24cffac6611ec5bf7f76f
Source noteuspto-grants-2016_09