Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475697Generated: October 29, 2026

Sodium Hydroxide → 4-(3-Pyridyl)cyclohex-3-en-1-one ethylene acetal

https://huagongshe.com/reaction/475697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Hydroxy-4-(3-pyridyl)cyclohexanone ethylene acetalHCID 20034904—
SolventPyridineHCID 1049—
Product4-(3-Pyridyl)cyclohex-3-en-1-one ethylene acetalHCID 20034903—

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637576B2
Source datasetuspto-grants-2014_01
ORD IDord-1390853779bd44ecbbf1baa9e0b0cea2
Source noteuspto-grants-2014_01