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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409480Generated: October 29, 2026

Benzyl Bromide → HCID 178501330, compound

https://huagongshe.com/reaction/409480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantCyclobutanecarboxylic acid, 3-hydroxy-, methyl esterHCID 12815112—
SolventDimethylformamideHCID 6228—
ProductHCID 178501330HCID 17850133015.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of cis-trans mixture of 3-hydroxy-cyclobutanecarboxylic acid methyl ester (1.30 g, 10 mmol) in DMF 13 mL is added NaH (50% in oil, 720 mg, 15 mmol) at 0° C. After stirring at 0° C. for 15 minutes, benzyl bromide (1.43 ml, 12 mmol) is added at 0° C. The mixture is stirred at room temperature for 2 hours and quenched with H2O. The solution is extracted with EtOAc. The organic layer is washed with H2O and brine, dried over MgSO4 and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent; hexane/EtOAc) to give trans-3-benzyloxy-cyclobutanecarboxylic acid methyl ester (340 mg, 15.4%). TLC (hexane/EtOAc, 5:1) Rf 0.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759365B2
Source datasetuspto-grants-2014_06
ORD IDord-81c8eed42ce64beea60a9559eae6bfbd
Source noteuspto-grants-2014_06