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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716072Generated: October 29, 2026

Acetonitrile → HCID 53671371, compound

https://huagongshe.com/reaction/716072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromoanilineHCID 11562—
ProductHCID 53671371HCID 5367137185%

Reaction Conditions

Temperature80 °C

Reaction Steps

K2CO3 (22.0 g, 159 mmol) was suspended in acetonitrile, the suspension was added with 3-bromoaniline (8.71 mL, 80.0 mmol) and allyl bromide (23.7 mL, 280 mmol), and the mixture was stirred at 80° C. for 14 hours. The reaction mixture was cooled to room temperature, then filtered through Celite, and sufficiently washed with ethyl acetate. The solvent was removed, and then the residue was purified by column chromatography (silica gel, ethyl acetate/hexane (1/40)) to obtain 3-bromo-N,N-diallylaniline (17.1 g, 67.9 mmol, yield 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187499B2
Source datasetuspto-grants-2015_11
ORD IDord-86da58d15a0a4aec962c87b02333bdb1
Source noteuspto-grants-2015_11