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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363673Generated: October 30, 2026

Ethanol → Aniline, N,N-diallyl- (8CI)

https://huagongshe.com/reaction/2363673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAnilineHCID 6115—
ReactantAllyl bromideHCID 7841—
ReactantSodium CarbonateHCID 10340—
SolventWaterHCID 962—
ProductAniline, N,N-diallyl- (8CI)HCID 9620275%

Reaction Conditions

Temperature19 °C

Reaction Steps

To a stirred solution of aniline (5.62 g, 60.36 mmol) in EtOH (200 ml) and water (50 ml) was added allyl bromide (17.33 g, 143.3 mmol) in one portion followed by solid Na2CO3 (6.69 g, 62.5 mmol). The yellow mixture was then heated under reflux for 17 h, left to cool to room temperature (19° C.) and the EtOH was removed under reduced pressure. The aqueous residue was extracted with Et2O (5×200 ml) and the combined organics were washed with brine (3×200 ml) and dried (Na2SO4). The solvent was removed under reduced pressure to give a brown oil that was distilled over KOH pellets to give the title compound (7.81 g, 75%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691979B2
Source datasetuspto-grants-2014_04
ORD IDord-e0dfc0b5dd104e9d958255f181956b88
Source noteuspto-grants-2014_04