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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906930Generated: October 29, 2026

Triphenylphosphine → HCID 67131823, compound

https://huagongshe.com/reaction/906930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 67131595HCID 67131595—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDiethylamineHCID 8021—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 67131823HCID 6713182368%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 2-{(SR)-1-[(3RS,4SR)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethoxy}-5-bromo-pyridine (128 mg, 0.253 mmol) and bis(triphenylphosphine) palladium(II) chloride (53 mg, 0.076 mmol) and triphenylphosphine (16.6 mg, 0.0632 mmol) and CuI (11 mg, 0.0578 mmol) in THF (3 mL) and diethylamine (1.5 mL) was added ethynyltrimethylsilane (0.108 mL, 0.759 mmol) under Ar. The mixture was heated at 85° C. over night. The reaction mixture was diluted with ethyl acetate and washed with aq.ammonium chloride solution two times. The separated organic phase was dried over anhydrous sodium sulfate and concentrated in vaccuo after filtration. The residue was purified by silica gel column chromatography (DCM) yielding 89.5 mg (68%) of the titled compound as a light yellow oil. ES-MS m/e: 523.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012998B2
Source datasetuspto-grants-2011_09
ORD IDord-1e58f6c5f08f497392fec00311cb0c59
Source noteuspto-grants-2011_09