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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784679Generated: October 31, 2026

2-(Di-tert-butylphosphino)biphenyl → (S)-1,4-di(t-butoxycarbonyl)-2-(4-((R)-3-hydroxy pyrrolidino)phenyl)piperazine

https://huagongshe.com/reaction/1784679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant(R)-3-PyrrolidinolHCID 2759337—
ReactantSodium t-butoxideHCID 23676156—
Reactant(S)-2-(4-bromophenyl)-1,4-di(t-butoxycarbonyl)piperazineHCID 53628944—
Catalystpalladium(II) acetateHCID 167845—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product(S)-1,4-di(t-butoxycarbonyl)-2-(4-((R)-3-hydroxy pyrrolidino)phenyl)piperazineHCID 6711738154.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A suspension of (S)-2-(4-bromophenyl)-1,4-di(t-butoxycarbonyl) piperazine (1.33 g, 3.00 mmol), (R)-3-pyrrolidinol (520 mg, 4.20 mmol), palladium acetate (27 mg, 0.12 mmol), 2-(di-t-butylphosphino)biphenyl (72 mg, 0.24 mmol), and sodium t-butoxide (808 mg, 8.41 mmol) in tert-butanol (20 mL) was heated at 90° C. for 3.5 h. After dilution with ethyl acetate, the resulting mixture was passed through a Celite column. The filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography eluting 10-50% ethyl acetate-hexane to afford (S)-1,4-di-(t-butoxycarbonyl)-2-(4-((R)-3-hydroxypyrrolidino) phenyl)piperazine (733 mg, 54.5%) as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504411B2
Source datasetuspto-grants-2009_03
ORD IDord-1a2856f551e44886a69872cb3f08fc44
Source noteuspto-grants-2009_03