Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-bromobenzoate | HCID 12081 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-(2-Methoxyethyl)piperazine | HCID 2734638 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl Benzoate | HCID 7150 | — |
Reaction Steps
To 10 ml of 1,4-dioxan is added 0.645 g (3.0 mmol) of methyl-4-bromobenzoate 0.519 g (3.6 mmol) of 1-(2-methoxy-ethyl-piperazine, 0.892 g (8.47 mmol) of potassium phosphate, 0.177 g (0.45 mmol) of 2-dicycohexylphosphino-2′-(N,N-dimethylamino)biphenyl and 0.137 g (0.15 mmol) tris-(benzylideneacetone)palladium (0). The resulting reaction mixture is stirred under argon for 5 hours at 100° C., then cooled to room temperature, diluted with ethyl acetate and filtered. The filtrate is washed once with H2O and once with brine, the organic layer separated and dried over Na2SO4. Purification of the crude product by flash chromatography (dichloromethane/methanol) yields 0.52 g of 4-[4-(2-methoxy-ethyl)-piperazin-1-yl)]benzoic acid methyl ester as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112589B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-eb71949554154dd0ac8446d9f681a659 |
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| Source note | uspto-grants-2006_09 |
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