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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217234Generated: October 30, 2026

Benzyl Bromide → HCID 178501330, compound

https://huagongshe.com/reaction/217234

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, NaH (50% in oil, 720 mg, 15 mmol) is added 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 AcOEt. 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 to give trans-3-benzyloxy-cyclobutanecarboxylic acid methyl ester (340 mg, 15.4%); TLC (hexane/AcOEt, 5:1) Rf 0.40, 1H NMR (400 MHz, chloroform-d) ppm 2.26-2.34 (m, 2H), 2.48-2.52 (m, 2H), 3.02-3.06 (m, 1H), 3.69 (s, 3H), 4.26-4.33 (m, 1H), 4.42 (s, 2H), 7.27-7.35 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193349B2
Source datasetuspto-grants-2012_06
ORD IDord-b29af3b0b60948b080eed8edcd26dff2
Source noteuspto-grants-2012_06