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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519762Generated: October 31, 2026

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

https://huagongshe.com/reaction/519762

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 numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-3008022454b24212b2a29d69cccb2339
Source noteuspto-grants-2015_08