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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-propylbenzene | HCID 136374 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58487948 | HCID 58487948 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247437B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-fcd042dc7b9647f4abd39442cab42d6b |
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| Source note | uspto-grants-2012_08 |
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