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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610715Generated: November 2, 2026

Phenylacetylene → HCID 19601754, compound

https://huagongshe.com/reaction/610715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 102356231HCID 102356231—
SolventBenzeneHCID 241—
ProductHCID 19601754HCID 1960175443.9%

Reaction Steps

Hydrosilation of phenylacetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of Pt(C2H4)(PPh3)2. Into the same apparatus as described in Example 1 were add 0.99 g of bis(dichlorosilyl)trichlorosilylmethane, 0.101 g of Pt(C2H4)(PPh3)2, and 25 ml of dried benzene forming a mixture. To this mixture at reflux was added 0.32 ml of phenylacetylene over a 10 minute period. The resulting mixture was stirred for an additional 15 hours at reflux temperature and then the solvent removed. The residue was vacuum distilled at 67 Pa to give a mixture comprising 0.58 g of 1,1,3,3-tetrachloro-2-trichlorosilyl-4-phenyl-1,3-disilacyclopent-4-ene (TCD-GC area 43.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998649
Source datasetuspto-grants-1999_12
ORD IDord-cafd29a8814d41ccafb3a668a2cc600e
Source noteuspto-grants-1999_12