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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861064Generated: October 31, 2026

Phenol → 3-Phenoxy-cyclohex-2-enone

https://huagongshe.com/reaction/1861064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chlorocyclohex-2-en-1-oneHCID 568345—
SolventAcetoneHCID 180—
Product3-Phenoxy-cyclohex-2-enoneHCID 3654216—

Reaction Steps

To a stirred solution of 3-chloro-cyclohex-2-enone (3.00g, 23.0 mmol) and phenol (2.16 g, 23.0 mmol) in 25 mL of acetone was added powdered, anhydrous K2CO3 (3.81 g, 27.6 mmol). After refluxing for 18 h, the mixture was cooled and filtered. The filtrate was concentrated under reduced pressure and chromatographed on silica gel eluting with hexanes/EtOAc (4:1) to give 3-phenoxy-cyclohex-2-enone as a white solid: 1H NMR (CDCl3) δ 2.10 (quint, 2H, J=6.3 Hz), 2.40 (t, 2H, J=6.2 Hz), 2.68 (t, 2H, J=6.3 Hz), 5.14 (s, 1H), 7.05 (d, 2H, J=7.5 Hz), 7.26 (t, 1H, J=7.3 Hz), 7.41 (t, 2H, J=7.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531491B1
Source datasetuspto-grants-2003_03
ORD IDord-81ed9cb20f0b44d1849c6473b2a3978a
Source noteuspto-grants-2003_03