HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 3-Phenoxy-cyclohex-2-enone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chlorocyclohex-2-en-1-one | HCID 568345 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Phenoxy-cyclohex-2-enone | HCID 3654216 | — |
Reaction Steps
To a stirred solution of 3-chloro-cyclohex-2-enone (3.00 g, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141587B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-9e254df8eca048a397b45b9e112ddb37 |
| Source note | uspto-grants-2006_11 |