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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046784Generated: November 1, 2026

3-Nitro-4-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)pyridine → 4-(3-Nitropyridin-4-yl)cyclohex-3-enone

https://huagongshe.com/reaction/2046784

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-4-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)pyridineHCID 59226542—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product4-(3-Nitropyridin-4-yl)cyclohex-3-enoneHCID 5922653685%

Reaction Steps

A mixture of 3-nitro-4-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)pyridine (1.0 equiv.) in 20% TFA in CH2Cl2 (0.2 M) was stirred at room temperature overnight. The solvents were removed under reduced pressure. The residue was dissolved with ethyl acetate (200 mL), and washed with sat NaHCO3 (30 mL), and sat NaCl (30 mL). The organic was dried with MgSO4, filtered and concentrated to give 4-(3-nitropyridin-4-yl)cyclohex-3-enone (85%). The crude product was used to next step without further purification. LC/MS (m/z): MH+=218.9, Rt=0.60

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592455B2
Source datasetuspto-grants-2013_11
ORD IDord-d7584e87e97e4bdeab9e94dd644cf0c0
Source noteuspto-grants-2013_11