Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1688728Generated: November 2, 2026

Acetone → 4-(2-Hydroxy-2-methylpropoxy)cyclohexanone

https://huagongshe.com/reaction/1688728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
Reactant1-(1,4-Dioxaspiro[4.5]dec-8-yloxy)-2-methylpropan-2-olHCID 67009178—
SolventWaterHCID 962—
Product4-(2-Hydroxy-2-methylpropoxy)cyclohexanoneHCID 6700891473%

Reaction Steps

A mixture of 1-(1,4-dioxaspiro[4.5]dec-8-yloxy)-2-methylpropan-2-ol (5.53 g), 3N hydrochloric acid (30 mL) and acetone (30 mL) was stirred at room temperature for 16 hr. The reaction mixture was diluted with water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography [eluent: hexane/ethyl acetate=80/20→60/40 (volume ratio)] to give the title compound as a colorless oil (3.25 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148383B2
Source datasetuspto-grants-2012_04
ORD IDord-31ed946d7dbc47e3b3b0068e81af2f92
Source noteuspto-grants-2012_04