HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884149Generated: October 30, 2026
Water → t-Butyl 4-[4-(5-nitropyridin-2-yloxy)benzyl]piperazine-1-carboxylate
https://huagongshe.com/reaction/884149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-(4-Chloromethylphenoxy)-5-nitropyridine | HCID 68526143 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | t-Butyl 4-[4-(5-nitropyridin-2-yloxy)benzyl]piperazine-1-carboxylate | HCID 68526806 | — |
Reaction Steps
To a solution of 2-(4-chloromethylphenoxy)-5-nitropyridine (12.32 g, 47 mmol) in DMF (120 mL) were added triethylamine (19.4 mL, 140 mmol) and t-butyl piperazine-1-carboxylate 11.27 g, 61 mmol), and the resulting solution was stirred for 3 hours at 50° C. Water was added to the residue, and extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine. The ethyl acetate layer was dried over anhydrous magnesium sulfate, and evaporated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1), to thereby yield 11.26 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236826B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-498ce6d889154815b55ad8fdd5e1a1fb |
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| Source note | uspto-grants-2012_08 |
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