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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765548Generated: October 31, 2026

Benzyl Bromide → HCID 21107328, compound

https://huagongshe.com/reaction/1765548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21107316HCID 21107316—
SolventDimethylformamideHCID 6228—
ProductHCID 21107328HCID 2110732893.4%

Reaction Steps

To a suspension of sodium hydride (60%, 0.7 g, 16.8 mmol) in anhydrous N,N-dimethylformamide (80 ml) was added 5-allyl-quinolin-6-ol (intermediate 5) (2.68 g, 14 mmol) slowly at room temperature. The reaction mixture was stirred for 1 hour, then benzyl bromide (2.57 ml, 21 mmol) was added. The mixture was allowed to stir for 1.5 hrs at room temperature, quenched with water and extracted with methylene chloride. The organic layer was washed with water, dried over anhydrous sodium sulfate and filtered. The solvent was removed under vacuum. Chromatography (30% hexanes-ethyl acetate) afforded 3.6 g (92%) of 5-allyl-6-benzyloxy-quinoline as a light brown oil. MS ESI m/z 276 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07227023B2
Source datasetuspto-grants-2007_06
ORD IDord-bb4c30f5ce0c4853956763fcced2dee6
Source noteuspto-grants-2007_06