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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567883Generated: October 29, 2026

Triphenylphosphine → HCID 21263166, compound

https://huagongshe.com/reaction/567883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 23431845HCID 23431845—
CatalystCopper iodideHCID 83717—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 21263166HCID 212631662,664.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-7,9-dimethoxy-10,11-dihydrodibenz[b,f]oxepin-10-one 500 mg (F. W. 349.18, 1.43 mmol) prepared in the first stage of Production Example 79, triphenylphosphine 75 mg (F. W. 262.29, 0.062 mmol), trisbenzyldene acetone dipalladium chloroform complex 74 mg (F. W. 1035.08, 0.015 mmol), diisopropylethylamine 575 μl (F. W. 98.22, d=0.742, 2.86 mmol), ethynyl trimethylsillane 350 μl (F. W. 98.22, d=0.742, 2.86 mmol) and copper iodide 27.5 mg (F. W. 190.44, 0.143 mmol) were dissolved in N-methyl-2-pyrrolidone (5 ml) and, after substituting with argon atmosphere, they were stirred with heating at 80° C. for one hour. The reaction mixture was diluted with ethyl acetate and washed with water and saturated sodium chloride solution. The organic layer was dried and concentrated and the resulting residue was purified by a silica gel column chromatography to give the title compound 420 mg (F. W. 367.419, 66%). The peaks of this compound in 1H-NMR (400 MHz, CDCl3) were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180659B2
Source datasetuspto-grants-2001_01
ORD IDord-6d299c3be5b34cc293512871c358c2e4
Source noteuspto-grants-2001_01