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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667130Generated: November 1, 2026

tert-Butyl 4-(2-bromoethyl)piperazine-1-carboxylate → Tert-butyl 4-(2-(3,3-bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl)ethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1667130

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2-bromoethyl)piperazine-1-carboxylateHCID 15946441—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3,3-Bis(4-fluorophenyl)pyrrolidin-2-oneHCID 67358565—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(2-(3,3-bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl)ethyl)piperazine-1-carboxylateHCID 67359885—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 3,3-bis(4-fluorophenyl)pyrrolidin-2-one (Example 58B, 1.37 g, 5.00 mmol) in tetrahydrofuran (30 mL) was added potassium t-butoxide (1.0 M in tetrahydrofuran) (7.5 mL, 7.5 mmol) followed by the product from Example 63A (1.47 g, 5.00 mmol). The reaction mixture was heated at 75° C. for 18 hours. The reaction was concentrated, diluted with ethyl acetate, washed with water and brine, dried with MgSO4, filtered and concentrated. The residue was purified with silica gel chromatography eluting with 3% methanol/dichloromethane to give the title compound. MS (DCI) m/z 486.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044069B2
Source datasetuspto-grants-2011_10
ORD IDord-2e93e0abe194410db3b05be3b3510765
Source noteuspto-grants-2011_10