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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436Generated: October 24, 2026

1-Bromo-4-iodobenzene → 1-(4-Bromophenyl)-cis-3,5-dimethylpiperazine

https://huagongshe.com/en/reaction/436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactantrel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
ReagentSodium t-butoxideHCID 23676156—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Bromophenyl)-cis-3,5-dimethylpiperazineHCID 6673036144.14%

Reaction Conditions

Temperature90 °C

Reaction Steps

sodium 2-methylpropan-2-olate (0.510 g, 5.30 mmol) was added to (2R,6S)-2,6-dimethylpiperazine (0.605 g, 5.30 mmol) in dioxane (40 mL) at 21°C under nitrogen. Stirred for 5 mins. 1-bromo-4-iodobenzene (1 g, 3.53 mmol) added, followed by diacetoxypalladium (0.079 g, 0.35 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.409 g, 0.71 mmol). Reaction evacuated and refilled with nitrogen several times. Heated at 90C for 18hours. left to cool o/w. The reaction mixture was diluted with EtOAc (250 mL), and washed sequentially with water (150 mL). The organic layer was dried over Na2SO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 30% MeOH in EtOAc. Pure fractions were evaporated to dryness to afford (3S,5R)-1-(4-bromophenyl)-3,5-dimethylpiperazine (0.420 g, 44.1 %) as a yellow solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-609b92e7f381461a936ff9653aaca797
Source note750 AstraZeneca ELN dataset