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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350399Generated: November 3, 2026

Triphenylphosphine → HCID 58860671, compound

https://huagongshe.com/reaction/1350399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Chloro-4-iodobenzeneHCID 12510—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant(S)-1,4-dibenzyl-2-vinylpiperazineHCID 17759473—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
ProductHCID 58860671HCID 5886067169%

Reaction Steps

Combine (S)-1,4-dibenzyl-2-vinyl-piperazine (5.0 g, 17.10 mmol) and 9-borabicyclo[3.3.1]nonane (136.8 ml, 68.39 mmol, 0.5 M in THF) and stir at ambient temperature. After 24 hrs, add 1-iodo-4-chloro-benzene (6.12 g, 25.65 mmol), triphenylphosphine (717.5 mg, 2.74 mmol), tetrakis(triphenylphosphine) palladium(0)(395.1 mg, 0.34 mmol), and 3N NaOH (14.0 ml) and stir at 60°. After 22 hrs, remove the THF under vacuum, stir the residue in 2N NaOH, and extract with diethyl ether. Wash the organic with 1N H2SO4 then adjust the aqueous to pH 14. Extract the aqueous with diethyl ether and combine, wash (brine), dry (sodium sulfate), and reduce the extracts to residue. Recrystallize the residue in warm ethanol to give 4.76 g (69%) of the title compound: mp 87°–90°; mass spectrum (ion spray): m/z=405.4 (M+1); Analysis for C26H29ClN2: calcd: C, 77.11; H, 7.22; N, 6.92; found: C, 76.93; H, 7.06; N, 7.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-1396d67339e8445bb221376d2a8151e6
Source noteuspto-grants-2007_05