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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39712Generated: October 28, 2026

Allyl bromide → N-allyl-3-methoxyaniline

https://huagongshe.com/reaction/39712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant3-MethoxyanilineHCID 10824—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-allyl-3-methoxyanilineHCID 14069075—

Reaction Steps

To 10 mL of a tetrahydrofuran solution containing 1.0 g of m-anisidine, 1.2 mL of triethylamine and 0.70 mL of allyl bromide were added under cooling with ice. The reaction mixture was stirred for 30 minutes. Water and ethyl acetate were added thereto. The organic layer was separated, and the aqueous layer was separated with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=5:1] to obtain 0.36 g of a yellow oily substance, N-allyl-3-methoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-8a56c0618a2e429185b86f3db82820d5
Source noteuspto-grants-2013_09