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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722705Generated: October 31, 2026

Propargyl bromide → 4-Fluoro-N-(prop-2-yn-1-yl)aniline

https://huagongshe.com/reaction/1722705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantEthyl AcetateHCID 8857—
Reactant4-FluoroanilineHCID 9731—
ReactantDiisopropylethylamineHCID 81531—
SolventTolueneHCID 1140—
Product4-Fluoro-N-(prop-2-yn-1-yl)anilineHCID 14650036—

Reaction Steps

A solution of 9.47 ml (0.1 mol) of 4-fluorobenzenamine, 16.36 g (0.11 mol) of an 80% solution of 3-bromo-1-propyne in toluene, and 17.43 ml (0.11 mol) of N-ethyl-N-(1-methylethyl)-2-propanamine in 350 ml of toluene is heated at 90° C. for three hours. Ethyl acetate is added to the reaction suspension, and it is washed three times with water. The organic layer is separated, dried (magnesium sulfate), and concentrated to give 15.5 g of a dark brown liquid. This is applied to a column of 1 kg of flash silica gel packed in heptane-dichloromethane (5:1). Elution with the same solvent gives 9.09 g (61%) of the product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857530
Source datasetuspto-grants-1989_08
ORD IDord-f767ab45708a4eb6b03112c05d2a8208
Source noteuspto-grants-1989_08