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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987553Generated: October 25, 2026

Acetic Acid → Benzyl 4-isobutyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/1987553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ProductBenzyl 4-isobutyl-1-piperazinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550503B2
Source datasetuspto-grants-2009_06
ORD IDord-d1ff54c045f746ca80c686c471279c97
Source noteuspto-grants-2009_06