HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092055Generated: October 25, 2026
Methyl 4-bromobenzoate → Methyl 4-(4-acetylpiperazin-1-yl)benzoate
https://huagongshe.com/reaction/1092055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-bromobenzoate | HCID 12081 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-(4-acetylpiperazin-1-yl)benzoate | HCID 57440409 | 56.2% |
Reaction Steps
A deoxygenated suspension of 1-acetylpiperazine (0.308 g, 2.40 mmol), methyl 4-bromobenzoate (0.430 g, 2 mmol), tri-potassium orthophosphate (0.594 g, 2.80 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (0.164 g, 0.40 mmol) and tris(dibenzylideneacetone)dipaladium(0) (0.092 g, 0.10 mmol) in toluene (10 mL) was stirred at 100° C., over a period of 24 h under nitrogen. The cooled reaction mixture was filtered and evaporated to give crude product. The crude product was purified by silica column chromatography, eluting with a gradient 0-5% MeOH in DCM. Pure fractions were evaporated to dryness to afford methyl 4-(4-acetylpiperazin-1-yl)benzoate (0.295 g, 56.2%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129391B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-5a63809dbce14385b7d4c2ae6f2d3eb1 |
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| Source note | uspto-grants-2012_03 |
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