HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436979Generated: October 25, 2026
Acetic Acid → Benzyl 4-isobutyl-1-piperazinecarboxylate
https://huagongshe.com/reaction/1436979
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl piperazine-1-carboxylate | HCID 643495 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Product | Benzyl 4-isobutyl-1-piperazinecarboxylate | HCID 23069811 | — |
Reaction Steps
Benzyl 1-piperazinecarboxylate (1.1 g, 5.00 mmol) and isobutylaldehyde (0.91 mL, 10.0 mmol) were dissolved in 30 mL of tetrahydrofuran, and acetic acid (0.57 mL, 10.0 mmol) and sodium triacetoxyborohydride (2.11 g, 10.0 mmol) were added thereto, and the reaction mixture was stirred at room temperature for two hours. The reaction mixture was mixed with a 1N aqueous solution of sodium hydroxide, extracted with ethyl acetate twice, and the combined organic layers were washed with brine once. The mixture was dried over anhydrous sodium sulfate and evaporated. The resulting residue was purified by silica gel column chromatography (Fuji Silysia, NH Silica gel; ethyl acetate:hexane=50:50) to give benzyl 4-isobutylpiperazin-1-carboxylate (1.05 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07619100B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-d88efff1693c446fbf8bfea5660d42ef |
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| Source note | uspto-grants-2009_11 |
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