HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(3-Pyridyl)cyclohex-3-en-1-one ethylene acetal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Hydroxy-4-(3-pyridyl)cyclohexanone ethylene acetal | HCID 20034904 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(3-Pyridyl)cyclohex-3-en-1-one ethylene acetal | HCID 20034903 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Thionyl chloride (45 mL, 622.5 mmol) was slowly added to a solution of 4-hydroxy-4-(3-pyridyl)cyclohexanone ethylene ketal (prepared as in step a, 29.3 g, 124.5 mmol) in pyridine (250 mL) at −10° C. After stirring at 0° C. for 2.5 h, the reaction mixture was poured onto ice and adjusted to pH 8 with 2 N NaOH. The aqueous layer was extracted with CH2Cl2 (100 mL×3) and the combined organic layers were washed with brine (200 mL), dried with MgSO4, and concentrated in vacuo to afford crude 4-(3-pyridyl)cyclohex-3-en-1-one ethylene ketal, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637576B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-1390853779bd44ecbbf1baa9e0b0cea2 |
| Source note | uspto-grants-2014_01 |