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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610712Generated: November 1, 2026

Acetylene → HCID 19601757, compound

https://huagongshe.com/reaction/610712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
ReactantHCID 102356231HCID 102356231—
ProductHCID 19601757HCID 1960175781.4%

Reaction Steps

Hydrosilation of acetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of H2PtCl6. To a 50 ml, three-necked, dried, flask equipped with a magnetic stirrer was added 200 μl of a 0.1 M H2PtCl6 /isopropyl alcohol (IPA) solution. The flask was placed under dry nitrogen atmosphere and the IPA removed under vacuum. Then, 6.29 g of bis(dichlorosilyl)trichlorosilylmethane and 25 ml of dried benzene were added to the flask forming a solution. The solution was maintained at reflux temperature and acetylene gas fed into the solution at a rate of 90 ml per minute for 10 hours. The resulting products were vacuum distilled at 67 Pa to yield 6.36 g of 1,1,3,3-tetrachloro-2-trichlorosilyl-1,3-disilacyclopent-4-ene (TCD-GC are 81.4%) (TCD-GC =gas chromatography using a thermal conductivity detector) and 1,1,3,3-tetrachloro-2-trichlorosilyl-1,3-disilacyclopentane (TCD-GC 4.2%) as a mixture. The structure of 1,1,3,3-tetrachloro-2-trichlorosilyl-1,3-disilacyclopent-4-ene was confirmed by 1H-NMR (CDCl3, ppm): 1.52 (s, 1H, SiCHSi), 7.42 (s, 2H, CH=CH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998649
Source datasetuspto-grants-1999_12
ORD IDord-2863b678cc274116adb83d1dafb7414a
Source noteuspto-grants-1999_12