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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634865Generated: October 29, 2026

Hydrochloric Acid → Ethyl 2-(3-chlorophenoxy)acetate

https://huagongshe.com/reaction/634865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
Reactant3-ChlorophenolHCID 7933—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(3-chlorophenoxy)acetateHCID 73542287.2%

Reaction Steps

Acetone (320 ml), 75 g (450 mmol) of ethyl bromoacetate, and 40.0 g (310 mmol) of 3-chlorophenol were mixed together, then 69.8 g (505 mmol) of potassium carbonate was added. The mixture was mechanically stirred and heated to reflux for 4 h, and after cooling to room temperature, was poured into 350 mL of ethyl acetate. To this was then cautiously added 400 mL of 1M HCl, taking care to avoid excess foaming. The layers were separated and the aqueous layer was extracted with portions of ethyl acetate (3×200 mL). The combined organic layers were dried over MgSO4, filtered, concentrated, and the resulting solid was recrystallized from hexane to afford 58 g (87%) of 10 as a white solid, m.p.=39-40° C. 1H NMR δ 7.20-7.08 (m, 1 H), 6.95-6.82 (m, 2 H), 6.75-6.70 (m, 1 H), 4.53 (s, 2 H), 4.21 (q, J=7.2 Hz, 2 H), 1.23 (t, J=7.2 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184250B2
Source datasetuspto-grants-2001_02
ORD IDord-fc616e5b91c84719bc08d45f47d86e60
Source noteuspto-grants-2001_02