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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287836Generated: November 2, 2026

Benzyl Bromide → HCID 18705806, compound

https://huagongshe.com/reaction/2287836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18705875HCID 18705875—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductHCID 18705806HCID 18705806—

Reaction Steps

Sodium hydride (0.96 g, 24 mmol) was washed with hexane under nitrogen and suspended in DMF (10 mL). 2-(Dipropylamino)-2,3-dihydro-6-hydroxy-1H-inden-5-yl trifluoromethanesulfonate (69, 7.6 g, 20 mmol) in DMF (30 mL) was added dropwise at 0-5° C. over 30 min and the mixture stirred 30 min. Benzyl bromide (5.13 g, 30 mmol) in DMF (5 mL) was added and the resulting mixture was stirred 1 h. The reaction was quenched with saturated NaHCO3 and extracted with EtOAc. The organic layer was washed with water, brine, dried (MgSO4), filtered and concentrated to give the crude product. Chromatographic purification yielded pure product 70 as an oil that was converted into the HCl salt and crystallized from EtOAc/MeOH/hexane to give a white solid (mp 162-163° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06084130
Source datasetuspto-grants-2000_07
ORD IDord-c425d38d51a04f9093ee22d7cbe1c95f
Source noteuspto-grants-2000_07