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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429717Generated: October 30, 2026

Hydrochloric Acid → 4-(2-Methylphenyl)cyclohexanone

https://huagongshe.com/reaction/429717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant8-(o-Tolyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 54450779—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
Product4-(2-Methylphenyl)cyclohexanoneHCID 1835266935%

Reaction Steps

A solution of 4-(2-methylphenyl)-4-hydroxycyclohexanone ethylene ketal from the preceding step in 800 mL dioxane was treated with 16 mL concentrated hydrochloric acid and 30 grams 10% palladium-on-carbon under 35 p.s.i. hydrogen for 24 hours, then filtered through Celite to remove the catalyst. The filtrate was treated with 230 mL water and stirred at room temperature for 48 hours. The solution was evaporated, the pH adjusted to 8 with saturated aqueous sodium bicarbonate solution, and extracted with methylene chloride. The organic layer was dried over sodium sulfate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/hexanes as eluent to afford 33.3 grams (35%) of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319915B1
Source datasetuspto-grants-2001_11
ORD IDord-90f69e579b1f4065802ba9a229f178bf
Source noteuspto-grants-2001_11