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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170296Generated: October 26, 2026

Isopropenyl acetate → 1-(4-Bromo-2,6-dichloro-phenyl)-propan-2-one

https://huagongshe.com/reaction/2170296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
ReactantTert-Butyl nitriteHCID 10906—
Reactant4-Bromo-2,6-dichloroanilineHCID 69680—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product1-(4-Bromo-2,6-dichloro-phenyl)-propan-2-oneHCID 8978316098.3%

Reaction Steps

In a 50 ml three-neck flask equipped with mechanical stirring, cooling funnel, dropping funnel and thermometer under nitrogen at ambient temperature filled with acetonitrile (10 ml), were added cuprous oxide (1.5 g, 0.018 mol), isopropenyl acetate (13.6 ml, 0.125 mol) and tert-butyl nitrite (1.7 ml, 0.0125 mol). The resulting red suspension is stirred for 15 min at ambient temperature. A solution of 4-bromo-2,6-dichloroaniline (2.0 g, 0.0083 mol), dissolved in acetonitrile (15 ml) was added dropwise over a period of 20 minutes. During the addition, bubbling was observed. The mixture was stirred at 40° C. for 20 hours. The red crude mixture was passed through celite to remove solid particles and concentrated under reduce pressure to give a brown solid. The residue was dissolved in dichloromethane (120 ml) and washed with water (2×50 ml) and brine (40 ml). Organics were dried over sodium sulfate and concentrated under reduced pressure to give crude 1-(4-bromo-2,6-dichloro-phenyl)-propan-2-one (2.3 g) as a dark brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051272B2
Source datasetuspto-grants-2015_06
ORD IDord-d0fbc6b7c87c4af1a4951472279149aa
Source noteuspto-grants-2015_06