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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595955Generated: October 31, 2026

Phenylacetylene → HCID 21705263, compound

https://huagongshe.com/reaction/1595955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 13789611HCID 13789611—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 21705263HCID 21705263131.5%

Reaction Steps

A solution of 3,3′-dibromobenzil (5.0 g, 0.0136 mol) and phenylacetylene (3.47 g, 0.0340 mol) in triethylamine (30 mL) is deaerated by bubbling nitrogen through the solution for ten minutes. (PPh3)2PdCl2 (0.067 g, 0.0001 mol) is then added, and the reaction mixture heated at reflux overnight. The mixture is concentrated to dryness, then taken up in CH2Cl2 (100 mL), washed sequentially with 1 M HCl, saturated aqueous NaHCO3 and dried (Na2SO4), then concentrated, giving 3.67 g (66 percent) product as a white solid: m.p. 144° C. to 145° C.; 1H NMR (CDCl3) δ 8.12 (s, 2H), 7.96 (d, J=7.9 Hz, 2H), 7.81 (d, J=7.7 Hz, 2H), 7.52 (m, 6H), 7.36 (m, 6H); 13C NMR (CDCl3) δ 192.83, 137.40, 132.82, 131.52, 129.04, 128.58, 128.25, 124.50, 122.37, 91.11, 87.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288188B1
Source datasetuspto-grants-2001_09
ORD IDord-00281e43d1bb490d9dd289e5831a770c
Source noteuspto-grants-2001_09