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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290979Generated: October 29, 2026

4-Nitrophenol → Tert-butyl 2-(4-nitrophenoxy)acetate

https://huagongshe.com/reaction/1290979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(4-nitrophenoxy)acetateHCID 2206104386.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Nitrophenol (13.9 g, 100 mmol) was dissolved in N,N-dimethylformamide (20 ml), and t-butyl bromoacetate (29.3 g, 150 mmol) and potassium carbonate (27.6 g, 200 mmol) were added, which was followed by stirring at 70° C. for 4 hours. The reaction mixture was diluted with ethyl acetate (100 ml), washed with water, and the aqueous layer was extracted with ethyl acetate. The extract and the previously-obtained organic layer were combined. The mixture was washed with water and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure, and the residue was purified by silica gel column chromatography. (n-hexane/ethyl acetate=5/1) and recrystallized from a mixed solvent of ethyl acetate and n-hexane to give 21.8 g of t-butyl 4-nitrophenoxyacetate as pale-yellow crystals (86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753670
Source datasetuspto-grants-1998_05
ORD IDord-82caed2520de465798bf498b0136a67f
Source noteuspto-grants-1998_05