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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966083Generated: October 30, 2026

Benzyl Bromide → HCID 178500717, compound

https://huagongshe.com/reaction/1966083

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 numberUS08420641B2
Source datasetuspto-grants-2013_04
ORD IDord-33b801cf01c44eb59ba6eb853b332f73
Source noteuspto-grants-2013_04