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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610719Generated: November 2, 2026

Diphenylacetylene → HCID 19601750, compound

https://huagongshe.com/reaction/610719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylacetyleneHCID 10390—
ReactantHCID 102356231HCID 102356231—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
ProductHCID 19601750HCID 1960175025%

Reaction Steps

Hydrosilation of diphenylacetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of Pd(PPh3)4. Into the same apparatus as described in Example 1 were add 0.98 g of bis(dichlorosilyl)trichlorosilylmethane, 0.101 g of Pd(PPh3)4, and 25 ml of dried benzene to form a mixture. The mixture was brought to reflux temperature and 0.52 g of diphenylacetylene in 10 ml of benzene were added over a 30 minute period. The mixture was stirred at reflux temperature for an additional 18 hours and then the solvent removed at atmospheric pressure. The residue was vacuum distilled to yield a mixture comprising 0.417 g of 1,1,3,3-tetrachloro-2-trichlorosilyl-4,5-diphenyl-1,3-disilacyclopentane (TCD-GC area 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998649
Source datasetuspto-grants-1999_12
ORD IDord-6c47efcc63f2450cb363cc528d8e7fd3
Source noteuspto-grants-1999_12