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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715772Generated: October 30, 2026

p-Fluoronitrobenzene → 1,1-Dimethylethyl (3R)-3-(4-nitrophenoxy)-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/715772

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylateHCID 6544479—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product1,1-Dimethylethyl (3R)-3-(4-nitrophenoxy)-1-pyrrolidinecarboxylateHCID 53255708—

Reaction Conditions

Temperature40 °C

Reaction Steps

(R)-Tert-butyl 3-hydroxypyrrolidine-1-carboxylate (10 g, 53.4 mmol) was dissolved in 1-fluoro-4-nitrobenzene (13.94 g, 99 mmol). An aqueous solution of 5.9N potassium hydroxide (77 ml, 452 mmol) was added followed by addition of tetrabutylammonium bromide (2.238 g, 6.94 mmol). The reaction mixture was stirred at 40° C. for 24 hours, cooled, diluted with water and extracted with ethyl acetate. The combined organic layers were dried with sodium sulfate, filtered and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187472B2
Source datasetuspto-grants-2015_11
ORD IDord-7fc6041628394057be052f88c02b69c6
Source noteuspto-grants-2015_11