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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888186Generated: October 30, 2026

1-Bromo-4-propylbenzene → HCID 58487948, compound

https://huagongshe.com/reaction/888186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-propylbenzeneHCID 136374—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Methylpiperazine, (R)-HCID 7330434—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 58487948HCID 5848794836%

Reaction Steps

A mixture of (R)-2-methylpiperazine (3.00 g, 30.0 mmol, 1.0 eq), 1-bromo-4-propylbenzene (627 g, 31.5 mmol, 1.05 eq.), (+/−)-BINAP (747 mg, 1.2 mmol, 0.04 eq.) and sodium tert-butoxide (4.32 g, 45.0 mmol, 1.5 eq.) in toluene (70 mL) was degassed for 15 min with N2. Palladium(II) acetate (337 mg, 1.5 mmol, 0.05 eq.) was then added at once. The reaction mixture was then heated to reflux for 16 h then cooled to RT. The mixture was then filtered on a bed of cellite and washed with Et2O. The combined organic layers were then washed with H2O (3×), dried over MgSO4, filtered and evaporated to give a dark to brown oil. This residue was purified by chromatography on silicagel (DCM/MeOH 80/20) to give the title product as yellow oil (2.35 g, 36%). M+(ESI): 2192.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247437B2
Source datasetuspto-grants-2012_08
ORD IDord-fcd042dc7b9647f4abd39442cab42d6b
Source noteuspto-grants-2012_08