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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromobenzoateHCID 90488—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)benzoic acidHCID 4482872642.2%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993555B2
Source datasetuspto-grants-2015_03
ORD IDord-a17195840b0e4533b2cc6ce490dc3ae0
Source noteuspto-grants-2015_03