HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32710Generated: October 29, 2026
tert-Butyl piperazine-1-carboxylate → 4-(3-Fluoro-4-trifluoromethyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/32710
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | 4-Chloro-2-fluoro-1-(trifluoromethyl)benzene | HCID 14227798 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(3-Fluoro-4-trifluoromethyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 59793628 | 61% |
Reaction Steps
To a mixture of sodium tert-butoxide (0.68 g, 6.9 mmol), palladium(II)acetate (11 mg, 0.05 mmol), 2-(di-t-butylphosphino)biphenyl (149 mg, 0.49 mmol), tert-Butyl-1-piperazine carboxylate (1.1 g, 5.9 mmol) and 4-chloro-2-fluorobenzotrifluoride (1 g, 4.94 mmol) was added degazed toluene (10 ml). The mixture was heated to 80° C. overnight. The mixture was cool to room temperature, diluted with ether, filtered and the filtrate was concentrated in vacuo. The residue was chromatographed over silica gel: eluent: Heptane/Ethylacetate 0-10% over 15 minutes to provide the title compound (1.05 g, 61%) as a white solid, MS (m/e): 349.2 (M+H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07427612B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-86ffc6494382430dbfc34be8ee112ab5 |
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| Source note | uspto-grants-2008_09 |
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