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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009160Generated: October 25, 2026

Water → 3-(Benzyloxy)cyclobutan-1-one

https://huagongshe.com/reaction/1009160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
Reactant(((1,3-Dibromopropan-2-yl)oxy)methyl)benzeneHCID 561824—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(Benzyloxy)cyclobutan-1-oneHCID 14932787—

Reaction Conditions

Temperature-20 °C

Reaction Steps

Methylsulfinyl(methylthio)methane (13 ml, 125 mmol) was dissolved in 250 ml THF and cooled to −20° C. n-Butyllithium (50 ml, 125 mmol) was added and the mixture was stirred for 3 h at −20° C. The mixture was cooled down to −78° C. and a solution of 1-((1,3-dibromopropan-2-yloxy)methyl)benzene (16.000 g, 52 mmol) was added. The reaction was stirred over night and allowed to warm up to RT. It was stirred for an additional 6 h at RT, hydrolyzed with water and extracted with EtOAc. The combined organic extracts were evaporated, dissolved in ether (50 ml) and treated with conc. HCl (10 ml) for 30 min at reflux. The mixture was neutralized with NaOH (10M) and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and evaporated. Glass col. Chrom. (10-50% EtOAc in Hex) gave 3-(benzyloxy)cyclobutanone as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973047B2
Source datasetuspto-grants-2011_07
ORD IDord-62640e8f36fa48219755166f11fe779e
Source noteuspto-grants-2011_07