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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-(2-bromoethyl)piperazine-1-carboxylate | HCID 15946441 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3,3-Bis(4-fluorophenyl)pyrrolidin-2-one | HCID 67358565 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(2-(3,3-bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl)ethyl)piperazine-1-carboxylate | HCID 67359885 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044069B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-2e93e0abe194410db3b05be3b3510765 |
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| Source note | uspto-grants-2011_10 |
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