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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852431Generated: November 2, 2026

3-Bromobenzyl bromide → HCID 86729349, compound

https://huagongshe.com/reaction/1852431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418385HCID 178418385—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86729349HCID 86729349—

Reaction Steps

To a solution of 1H-benzotriazole (0.52 g, 4.4 mmol) in THF (25 mL) was added potassium tert-butoxide (4.6 mL, 4.6 mmol, 1M in THF) followed by the addition of 1-bromo-3-(bromomethyl)benzene (1.0 g, 4.0 mmol). The solution was allowed to stir for 4 hours before the reaction was quenched with saturated aqueous NaHCO3 and diluted with EtOAc. The organic layer was separated and washed with brine, dried over anhydrous MgSO4, filtered, and concentrated to dryness in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 0-80% EtOAc/hexanes) to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962608B2
Source datasetuspto-grants-2015_02
ORD IDord-4c8ae5a2d547428cb75bba9088d714f1
Source noteuspto-grants-2015_02