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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610718Generated: November 1, 2026

Phenylacetylene → HCID 19601754, compound

https://huagongshe.com/reaction/610718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 102356231HCID 102356231—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
ProductHCID 19601754HCID 1960175443.9%

Reaction Steps

Hydrosilation of phenylacetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of Pd(PPh3)4. Into the same apparatus as described in Example 1 were added 1.0 g of bis(dichlorosilyl)trichlorosilylmethane, 0.102 g of Pd(PPh3)4, and 25 ml of dried benzene to form a mixture. The mixture was brought to reflux temperature and 0.32 ml of phenylacetylene added over a 10 minute period. The mixture was stirred at reflux temperature for an additional 8 hours and then the solvent removed at atmospheric pressure. The residue was vacuum distilled at 67 Pa to yield a mixture comprising 0.348 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-1340f3861ad140ebbd84ebccbdda447a
Source noteuspto-grants-1999_12