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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108831Generated: October 26, 2026

Potassium Carbonate → Tert-butyl (4-tert-butyl-3-chlorophenoxy)acetate

https://huagongshe.com/reaction/2108831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant4-tert-Butyl-3-chlorophenolHCID 13499472—
SolventAcetoneHCID 180—
ProductTert-butyl (4-tert-butyl-3-chlorophenoxy)acetateHCID 58640413126.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of potassium carbonate (994 mg, 7.2 mmol) and 4-tert-butyl-3-chlorophenol (440 mg, 2.4 mmol) in acetone (5 ml) was added t-butyl bromoacetate (370 mg, 1.9 mmol) was added and the mixture was refluxed at 60° C. for 14 hours. Filtrating of potassium carbonate, evaporation, and purification through silica gel column chromatography eluting with hexane/EtOAc (20:1 to 10:1) to furnish the tert-butyl (4-tert-butyl-3-chlorophenoxy)acetate (720 mg, 100%). The mixture of tert-butyl (4-tert-butyl-3-chlorophenoxy)acetate (720 mg, 2.4 mmol), TFA (2.0 ml), DCM (2.0 ml) was stirred for 5 hours at room temperature. After being concentrated in vacuo, the residue was triturated with hexane to furnish the title compound (582 mg, 100%) as a white solid. 1H NMR (300 MHz, CDCl3): δ 1.45 (9H, s), 4.67 (2H, s), 6.76 (1H, dd, J=2.6, 8.6 Hz), 6.96 (1H, d, J=2.6 Hz), 7.35 (1H, d, J=8.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514457B2
Source datasetuspto-grants-2009_04
ORD IDord-bbe265aa5f9f427889232584c30d740b
Source noteuspto-grants-2009_04