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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784695Generated: November 2, 2026

Borane;tetrahydrofuran → (S)-2-Benzylpiperazine

https://huagongshe.com/reaction/1784695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantCyclo(-Gly-Phe)HCID 7076549—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-BenzylpiperazineHCID 2076000140.3%

Reaction Steps

To a suspension of (S)-3-benzyl-2,5-dioxopiperazine (2.284 g, 11.18 mmol) in tetrahydrofuran (20 mL) was added borane-tetrahydrofuran complex (49 mL, 1.0 M solution in THF, 49 mmol) at room temperature. The resulting mixture was refluxed for several hours before it was quenched with methanol at 0° C. After concentration in vacuo, the residue was treated with 10% sodium hydroxide aqueous solution, which was extracted with dichloromethane thoroughly. The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated in vacuo to afford white crystals, which were washed with ether to yield (S)-2-benzylpiperazine (795 mg, 40.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504411B2
Source datasetuspto-grants-2009_03
ORD IDord-f1d429434cc449ce9006358226a97478
Source noteuspto-grants-2009_03