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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722706Generated: October 29, 2026

Propargyl bromide → Benzenamine, N-2-propyn-1-yl-4-(trifluoromethoxy)-

https://huagongshe.com/reaction/1722706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Trifluoromethoxy)anilineHCID 600848—
SolventTolueneHCID 1140—
SolventDichloromethane heptaneHCID 21907733—
ProductBenzenamine, N-2-propyn-1-yl-4-(trifluoromethoxy)-HCID 1465003766.2%

Reaction Steps

A solution of 8.86 g (50 mmol) of 4-(trifluoromethoxy)benzenamine, 8.18 g (55 mmol) of an 80% solution of 3-bromo-1-propyne in toluene, and 8.72 ml (50 mmol) of N-ethyl-N-(1-methylethyl)-2-propanamine in 200 ml of toluene is heated at 90° C. for eighteen hours. The suspension is cooled and treated with ethyl acetate. The suspension is washed several times with water. The ethyl acetate layer is separated, dried (magnesium sulfate), and concentrated to give a brown liquid. This is applied to a column of 1 kg of flash silica gel packed in n-heptane-dichloromethane (2:1). Elution with the same solvent gives 7.12 g (66.2%) of the product as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857530
Source datasetuspto-grants-1989_08
ORD IDord-97384ccf920e42868cb46dba25b9d8f7
Source noteuspto-grants-1989_08