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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610732Generated: November 1, 2026

Phenylacetylene → 1,3-Disilacyclopent-4-ene, 1,1,3,3-tetrachloro-4-phenyl-

https://huagongshe.com/reaction/610732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantBisdichlorosilylmethaneHCID 57370748—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
Product1,3-Disilacyclopent-4-ene, 1,1,3,3-tetrachloro-4-phenyl-HCID 1212144948.2%

Reaction Steps

Hydrosilation of phenylacetylene with bis(dichlorosilyl)methane in the presence of Pd(PPh3)4. Into the same apparatus as described in Example 1 were added 1 g of bis(dichlorosilyl)methane, 0.101 g of Pd(PPh3)4, and 20 ml of dried benzene. The flask content was heated to reflux and 0.52 ml of phenylacetylene was added over a ten minute period. The flask content was refluxed, with stirring, for another hours and then the solvent removed at atmospheric pressure. The products were vacuum distilled at 67 Pa to give a mixture comprising 0.89 g of 1,1,3,3-tetrachloro-4-phenyl-1,3-disilacyclopent-4-ene (TCD-GC area 48.2%) and 3,3,5,5-tetrachloro-1,7-diphenyl-3,5-disilahepta-1,6-diene (TCD-GC area6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998649
Source datasetuspto-grants-1999_12
ORD IDord-6434ff18243b4d17b167d364b033792b
Source noteuspto-grants-1999_12