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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377832Generated: October 27, 2026

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

https://huagongshe.com/reaction/1377832

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, 1H), 6.95-6.82 (m, 2H), 6.75-6.70 (m, 1H), 4.53 (s, 2H), 4.21 (q, J=7.2 Hz, 2H), 1.23 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665773
Source datasetuspto-grants-1997_09
ORD IDord-ad2f4c03402d49fc982ffaecdb3548c7
Source noteuspto-grants-1997_09