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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367246Generated: October 25, 2026

4-Nitrophenol → 1-(2-(4-Nitrophenoxy)ethyl)pyrrolidine

https://huagongshe.com/reaction/367246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantTriphenylphosphineHCID 11776—
Reactant1-PyrrolidineethanolHCID 76288—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
Product1-(2-(4-Nitrophenoxy)ethyl)pyrrolidineHCID 41985844.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 10 g of p-nitrophenol (72 mmol) in 100 mL dry THF was treated with 28.28 g (108 mmol) of triphenyl phosphine. The solution was cooled to 0° C. then treated with 18.78 g (108 mmol) diethyl azodicarboxylate. After stirring for 30 min at 0° C., 12.4 g (108 mmol) 1-(2-hydroxyethyl)pyrrolidine was added. The cooling bath was removed and the reaction allowed to stir overnight at ambient temperature. EtOAc was added (300 mL) and the mixture was extracted twice with 200 mL 1 N H2SO4. The combined extracts were washed twice with 200 mL EtOAc, made basic with 5 N NaOH and extracted three times with 150 mL EtOAc. The extracts were dried over MgSO4 and concentrated under vacuum to an oil which was purified by chromatography (SiO2 ; 1% MeOH in CHCl3) to recover 7.56 g (32 mmol, 44%) of the desired compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133262
Source datasetuspto-grants-2000_10
ORD IDord-b998848e56354337bd8174ffc65151d4
Source noteuspto-grants-2000_10