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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384477Generated: October 31, 2026

Hydrochloric Acid → 1-{2-[4-(Benzyloxy)phenyl]ethyl}cyclobutanol

https://huagongshe.com/reaction/384477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantCyclobutanoneHCID 14496—
ReactantMagnesiumHCID 5462224—
Reactant1-(Benzyloxy)-4-(2-bromoethyl)benzeneHCID 16638827—
SolventTetrahydrofuranHCID 8028—
Product1-{2-[4-(Benzyloxy)phenyl]ethyl}cyclobutanolHCID 5952756420.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of magnesium (35 mg) and THF (1.5 mL) was added one grain of iodine under nitrogen flow, followed by warming in an oil bath at 50° C. A solution of 1-(benzyloxy)-4-(2-bromoethyl)benzene (400 mg) in THF (3 mL) was added dropwise to the mixture over 20 minutes, and then the reaction liquid was heated under reflux for 4 hours. The reaction liquid was ice-cooled, and a solution of cyclobutanone (100 mg) in THF (4 mL) was added dropwise over 15 minutes, followed by stirring at room temperature for another 6 hours. The reaction liquid was adjusted to an acidic pH by adding 1M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9:1-1/1) to obtain 1-{2-[4-(benzyloxy)phenyl]ethyl}cyclobutanol (80 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-4ac691e7efd5497fa288597ef77a88f4
Source noteuspto-grants-2013_02