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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202252Generated: October 30, 2026

Water → HCID 178525083, compound

https://huagongshe.com/reaction/2202252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactantcis-Cyclobutane-1,3-dicarboxylic acidHCID 137582—
SolventDimethylformamideHCID 6228—
ProductHCID 178525083HCID 17852508323.6%
ProductHCID 178525084HCID 17852508422.9%

Reaction Steps

Potassium carbonate (575 mg, 4.16 mmol) and benzyl bromide (0.495 mL, 4.16 mmol) were added to a solution of cyclobutane-1,3-dicarboxylic acid (cis-trans mixture) (200 mg, 1.39 mmol) in DMF (4.0 mL) at room temperature, and the mixture was stirred overnight at room temperature. To the reaction mixture was added water at room temperature, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 0→5% ethyl acetate/hexane) to give dibenzyl cis-cyclobutane-1,3-dicarboxylate (106.3 mg, 0.328 mmol, 23.6%) as a less polar compound, and dibenzyl trans-cyclobutane-1,3-dicarboxylate (103.1 mg, 0.318 mmol, 22.9%) as a more polar compound, respectively. NMR spectrum of dibenzyl cis-cyclobutane-1,3-dicarboxylate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-57b17d7f91524ef0acd023bb917ea309
Source noteuspto-grants-2016_06