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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217248Generated: October 30, 2026

Benzyl Bromide → HCID 178500717, compound

https://huagongshe.com/reaction/217248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178500716HCID 178500716—
SolventDimethylformamideHCID 6228—
ProductHCID 178500717HCID 17850071740.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution trans-(3-hydroxy-cyclobutyl)-acetic acid methyl ester (168 mg, 1.17 mmol) in DMF (1.5 mL) is added, NaH (60% in oil, 70 mg, 1.75 mmol) at 0° C. After stirring at 0° C. for 15 minutes, benzyl bromide (167 uL, 1.40 mmol) is added at 0° C. The mixture is stirred at room temperature for 2 hours and quenched with H2O. The mixture is extracted with dichloromethane, and the organic layer is concentrated under reduced pressure. The obtained residue is purified by silica gel column chromatography to give trans-(3-benzyloxy-cyclobutyl)-acetic acid methyl ester (110 mg, 40%); ESI-MS m/z 235 [M+1]+, retention time 1.97 min (condition A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193349B2
Source datasetuspto-grants-2012_06
ORD IDord-7e35cc88492b4b118406cf317b84e25c
Source noteuspto-grants-2012_06