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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11316Generated: October 25, 2026

2-Chlorophenol → Ethyl 2-(2-chlorophenoxy)acetate

https://huagongshe.com/reaction/11316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorophenolHCID 7245—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductEthyl 2-(2-chlorophenoxy)acetateHCID 30282695%

Reaction Steps

To a stirred solution of 2-chlorophenol (6, 20.0 g, 156 mmol) in acetone (300 mL) under nitrogen at ambient temperature were added potassium carbonate (23.7 g, 171 mmol) and ethyl bromoacetate (7, 26.0 g, 156 mmol). The reaction mixture was then heated to reflux and stirred at this temperature under nitrogen for 7 hours. After cooling to ambient temperature, the reaction mixture was filtered to remove insolubles. The filtrate was then concentrated under reduced pressure to give 8 as highly viscous, light yellow oil (32.0 g, 95% yield, 95% pure by LCMS and 1H NMR), 1H NMR (400 MHz; CDCl3): δ 7.16 (m, 1H); 7.03 (m, 1H); 6.76 (m, 1H); 6.71 (m, 1H); 4.90 (s, 2H); 4.12 (q, 2H); 1.33 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098211B2
Source datasetuspto-grants-2006_08
ORD IDord-5026b40714514b03bf4016e828417bd4
Source noteuspto-grants-2006_08