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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1940362Erstellt: 26. Oktober 2026

Carbon Tetrachloride → 1,1',1''-(Chlorosilylidyne)tris(benzene)

https://huagongshe.com/reaction/1940362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon TetrachlorideHCID 5943—
EduktEthyleneHCID 6325—
EduktTriphenylsilanolHCID 69925—
EduktDisiloxane, 1,1,1,3,3,3-hexaphenyl-HCID 74587—
Eduktchromium (VI) trioxideHCID 10219390—
EduktHCID 178526121HCID 178526121—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelButyronitrileHCID 8008—
Produkt1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
ProduktHCID 178526121HCID 178526121—

Reaktionsschritte

Bistriphenylsilyl chromate is usually used as the catalyst of unsaturated hydrocarbon compound polymerization such as ethylene polymerization. With respect to its synthesis process, early in 1958, U.S. Pat. 7,863,891 disclosed a process wherein bistriphenylsilyl chromate can be obtained with a yield of 85% by reacting triphenylsilanol and chromium trioxide in glacial acetic acid at 50° C. for 10 minutes. L. M. Bakert et al disclosed a process wherein bistriphenylsilyl chromate can be obtained with a yield of about 60% by reacting triphenylsilanol and chromium trioxide in carbon tetrachloride at room temperature for 24 hours [J. Org. Chem., Vol. 85, No. 8, pp. 774-776, March 1970]. The former Czechoslovakia Patent CS 175856 disclosed a process wherein bistriphenylsilyl chromate can be obtained with a yield of 43-71% by reacting triphenylsilanol or triphenylsilyl ether and chromium trioxide in acetonitrile or propyl cyanide. However, the starting material triphenylsilanol used in the above processes is obtained by the hydrolysis of triphenylchlorosilane, so the process for the preparation of bistriphenylsilyl chromate is relatively complicated and the yield thereof is relatively low. The former Soviet Union Patent SU 689192 .disclosed a process wherein bistriphenylsilyl chromate can be obtained with a yield of 94% by reacting triphenylchlorosilane and potassium dichromate in glacial acetic acid at 40°-50° C. for 1.5 hours. The reaction equation thereof is as follows: ##STR1##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05698723
Quelldatensatzuspto-grants-1997_12
ORD IDord-8970a1da8b70416caac798b0fa5410c7
Quellennotizuspto-grants-1997_12