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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048502Generated: November 1, 2026

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

https://huagongshe.com/reaction/2048502

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 numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-d68b45ad9d7a4307951ae7af2a35d185
Source noteuspto-grants-2013_11