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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353342Generated: November 2, 2026

Sodium Hydroxide → 3-Cyclopentyl-2-(4-nitrophenyl)propionic acid

https://huagongshe.com/reaction/2353342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Cyclopentyl-2-(4-nitro-phenyl)-propionic acid ethyl esterHCID 11471849—
SolventMethanolHCID 887—
Product3-Cyclopentyl-2-(4-nitrophenyl)propionic acidHCID 11737121—

Reaction Steps

The title A compound, 3-cyclopentyl-2-(4-nitro-phenyl)-propionic acid ethyl ester (3.6 g, 12.3 mmol) is dissolved in 25 mL of methanol and aqueous NaOH (0.70 g, 17.5 mmol in 4 mL of water) is added and the mixture is stirred at RT overnight. The methanol is removed under reduced pressure and the residue is diluted with 100 mL of water and extracted with ether. The aqueous layer is then acidified with 1 N HCl (aq) and then extracted with ethyl acetate. The combined ethyl acetate layers are dried over anhydrous magnesium sulfate, filtered and reduced under vacuum to a crude orange oil. The crude oil is triturated with 100 mL of hexane/10-15 mL of ether to produce 3-cyclopentyl-2-(4-nitro-phenyl)-propionic acid as a solid: 1H NMR (400 MHz, CDCl3) δ 1.0-1.1 (m, 2H), 1.4-1.8 (m, 5H), 1.8-1.9 (m, 2H), 2.1-2.25 (m, 2H), 3.74 (t, 1H, J=7.8), 7.51 (d, 2H, J=8.8), 8.19 (d, 2H, J=8.8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750020B2
Source datasetuspto-grants-2010_07
ORD IDord-2a5370939fc94be2b8ef065396e6368a
Source noteuspto-grants-2010_07