HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389992Generated: October 25, 2026
Ethyl trifluoroacetate → Tert-butyl 4-(2,2,2-trifluoroacetyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1389992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Product | Tert-butyl 4-(2,2,2-trifluoroacetyl)piperazine-1-carboxylate | HCID 20294522 | 86.6% |
Reaction Steps
Ethyl trifluoroacetate (3.9 g, 0.027 mole) was added over 10 minutes to a warm (40° C.) stirred melt of 5.2 g (0.028 mole) 1-[1,1-dimethylethoxycarbonyl]piperazine. The mixture was heated at 120° C. for 2 hours, cooled to room temperature, treated with 1.0 g (0.007 mole) ethyl trifluoroacetate, and reheated for an additional 2 hours. The mixture was allowed to stand 18 hours at room temperature and then was evaporated in vacuo. The residue was dissolved in ether, passed through an alumina-packed column (2.2×16 cm), the eluent collected, washed with dilute aqueous HCl, dried (MgSO4), filtered, and evaporated in vacuo to yield 6.6 g yellow oil which solidified on standin g Recrystallization from hexane gave 6.0 g of white, crystalline solid, m.p. 66°-68° C. Calc. for C11H17F3N2O3 (282.26): C, 46.81; H, 6.07; N, 9.92. Found: C, 46.76; H, 6.40; N, 10.12.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04247549 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-fd649745ba654d83a09ee27cc1f1a1c5 |
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| Source note | uspto-grants-1981_01 |
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