HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25861Generated: October 25, 2026
o-Bromocumene → 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine
https://huagongshe.com/reaction/25861
Participants
| Role | Name | HCID | Charge |
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| Reactant | o-Bromocumene | HCID 23475 | — |
| Reactant | Dimethoxyethane ethanol | HCID 20074477 | — |
| Reactant | 4-(3'-Benzylphenyl)-3-(S)-isopropyl-piperazine | HCID 20760004 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | 2'-(diphenylphosphanyl)-N,N-dimethyl-[1,1'-biphenyl]-2-amine | HCID 2734939 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine | HCID 69129555 | 62.2% |
Reaction Steps
110.7 mg (0.38 mmol) 4-(3′-Benzylphenyl)-3-(S)-isopropyl-piperazine (88a), 123.5 mg (0.62 mmol, 1.65 eq.) 1-Bromo-2-isopropyl-benzene 11.7 mg (12.7 μmol, 0.034 eq.) Pd2(dba)3, 7.4 mg (19.3 μmol, 0.05 eq.) 2-Diphenylphosphino-2′-dimethylamino-biphenyl and 87.3 mg (0.91 mmol, 2.42 eq.) NaOt-Bu were dissolved in 5 ml dry toluene. The resulting mixture was heated under N2 at 80° C. for 15.5 h. After cooling to room temperature the mixture was diluted with ether and washed with brine. The comb. org. fractions were dried over Na2SO4 and evaporated. Column chromatography (hexanes/EtOAc (9+1)) yielded 96.5 mg (0.23 mmol, 62.20%) 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine (89) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858600B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-1b122892a0f943948cd06552bfdb562e |
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| Source note | uspto-grants-2005_02 |
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