Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852813Generated: October 29, 2026

Benzyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate → 5-[(1,2-Dioxo-1,2-dihydronaphth-4-yl)oxy]valeric Acid

https://huagongshe.com/reaction/852813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerateHCID 22647819—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product5-[(1,2-Dioxo-1,2-dihydronaphth-4-yl)oxy]valeric AcidHCID 2264782237%

Reaction Steps

Benzyl ester 2 (1.90 g, 5.22 mmol) was hydrogenated at 30 psi with Pd (400 mg) in ethyl acetate (120 mL) for 6 h. The catalyst was removed by filtration through celite, the solvent was evaporated in vacuo and the residue was oxidized with Ag2O (1.45 g, 6.25 mmol) in Et2O by stirring for 10 h. Following filtration and evaporation of the solvent the product was crystallized from benzene to afford 0.53 g of pure material. The mother liquor was purified by flash chromatography (CH2Cl2/MeOH 15:1), the product dissolved in CH2Cl2, extracted with aqueous NaHCO3 solution, acidified to pH 1 with 3% HCl and extracted back with CH2Cl2 to give additional 0.25 g of pure material (total yield 55%), mp 134-136° C.; 1H NMR (CDCl3) 8.12 (d, J=7.0 Hz, 1H), 7.87 (d, J=7.6 Hz, 1H), 7.70 (t, J=7.5 Hz, 1H), 7.59 (t, J=7.4 Hz, 1H), 7.27 (s, 1H), 4.18 (t, J=5.9 Hz, 2H), 2.51 (t, J=7.0 Hz, 2H), 1.75-2.15 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253207B2
Source datasetuspto-grants-2007_08
ORD IDord-76a0c7ab960f47d6b26f7cd5688ed690
Source noteuspto-grants-2007_08