HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872356Generated: November 3, 2026
Water → 1-(4-n-Octyloxyphenyl)-4-tert-butoxycarbonylpiperazine
https://huagongshe.com/reaction/1872356
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Hydroxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 11687740 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-n-Octyloxyphenyl)-4-tert-butoxycarbonylpiperazine | HCID 21182449 | — |
Reaction Steps
To a suspension of 1-(4-Hydroxyphenyl)-4-tert-butoxycarbonylpiperazine (3 g) and potassium carbonate (0.82 g) in N,N-dimethylformamide (15 ml) was added octyl bromide (1.87 ml). The mixture was stirred for 10 hours at 70° C. The reaction mixture was added to a mixture of water and ethyl acetate. The organic layer was taken, and dried over magnesium sulfate. The magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel, and eluted with (hexane : ethyl acetate=9:1). The fractions containing the object compound were combined, and evaporated under reduced pressure to give 1-(4-n-Octyloxyphenyl)-4-tert-butoxycarbonylpiperazine (2.71 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06107458 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-ea45349c290b44c88997654852ac3161 |
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| Source note | uspto-grants-2000_08 |
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