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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557Generated: October 23, 2026

p-Bromoacetophenone → Tert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylate

https://huagongshe.com/en/reaction/557

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylateHCID 2113619052.48%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a CEM MW vial, p-Bromoacetophenone (729 ml, 6.03 mmol),tert-Butyl 1-piperazinecarboxylate (1.684 g, 9.04 mmol),racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.375 g, 0.60 mmol),Palladium (II) acetate (0.135 g, 0.60 mmol),Cesium carbonate (3.93 g, 12.06 mmol) was taken in toluene (10 ml).The RM was subjected to MW power of 300W,temp 120°C for 45 minutes. The LCMS was checked showed the formation of required mass. Work-up: The RM was passed through hyflow bed and filtrate was evaporated and chrmatographed using Ethyl acetate hexane to obtain tert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylate (0.963 g, 52.5 %).

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-c7d1825ed35e4dffbc57a0b9b8fa9354
Source note750 AstraZeneca ELN dataset