HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416651Generated: October 25, 2026
Diisopropylethylamine → tert-Butyl 4-(3,3,3-trifluoropropyl)-1-piperazine-carboxylate
https://huagongshe.com/reaction/2416651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Bromo-1,1,1-trifluoropropane | HCID 2725114 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 4-(3,3,3-trifluoropropyl)-1-piperazine-carboxylate | HCID 22633053 | — |
Reaction Steps
To a solution of 1-(tert-butoxycarbonyl)piperazine (5.00 g) and N,N-diisopropylethylamine (4.68 ml) in N,N-dimethylformamide (13 ml) was added 1-bromo-3,3,3-trifluoropropane (5.00 ml) at 60° C. The mixture was stirred at 60° C. for 4 hours. The reaction mixture was poured into saturated aqueous sodium hydrogencarbonate solution and extracted with hexane. The organic layer was washed successively with saturated aqueous ammonium chloride solution, aqueous sodium hydrogencarbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated to give the title compound (5.38 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825200B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-facdc45277a04f8898a6d24147b75bce |
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| Source note | uspto-grants-2004_11 |
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