HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880284Generated: October 30, 2026
Ethyl 3-bromobenzoate → 3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)benzoic acid
https://huagongshe.com/reaction/880284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-bromobenzoate | HCID 90488 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)benzoic acid | HCID 44828726 | 42.2% |
Reaction Steps
The mixture of ethyl 3-bromobenzoate (500 mg, 2.33 mmol), tert-butyl piperazine-1-carboxylate (433 mg, 2.33 mmol) and NaOtBu (268 mg, 2.78 mmol), Pd2(dba)3 (20 mg, 0.034 mmol) and Xantphos (20 mg, 0.034 mmol) in anhydrous dioxane (10 mL) was heated to 110° C. for 10 h. The mixture was concentrated and the residue was partitioned in water, the solution was adjusted to pH=5, and extracted with DCM. The organic layer was washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated to afford the title compound that was used for next step (300 mg, Yield 42.2%). LCMS (m/z): 307.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993555B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a17195840b0e4533b2cc6ce490dc3ae0 |
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| Source note | uspto-grants-2015_03 |
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