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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243811Generated: November 2, 2026

Sodium Hydroxide → 3-(Ethoxycarbonyl)-5-(1-cyanocyclopentyl)benzoic acid

https://huagongshe.com/reaction/2243811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDiethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioateHCID 67318465—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3-(Ethoxycarbonyl)-5-(1-cyanocyclopentyl)benzoic acidHCID 67318462—

Reaction Steps

A solution of diethyl 5-(1-cyanocyclopentyl)benzene-1,3-dioate (0.33 g, 1.05 mmol) and NaOH (1N in H2O, 0.945 mL, 0.945 mmol) in 5 mL THF and 5 mL EtOH was stirred at rt overnight. The reaction mixture was concentrated, diluted with H2O and extracted with ether. The aqueous phase was made acidic with 1N HCl, extracted with EtOAc and the combined organic layers were washed with brine. Drying and solvent evaporation gave 3-(ethoxycarbonyl)-5-(1-cyanocyclopentyl)benzoic acid. 1H NMR (400 MHz, CD3OD) δ 8.58 (m, 1H), 8.35 (m, 2H), 4.43 (q, J=7.1 Hz, 2H), 2.51 (m, 2H), 2.18 (m, 2H), 2.05 (m, 4H), 1.42 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678783B2
Source datasetuspto-grants-2010_03
ORD IDord-481e130ceb9149ecb75d638a60c86022
Source noteuspto-grants-2010_03