[Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

Base Information

Chemical Name:[Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)
CAS No.:211561-64-7
Molecular Formula:BF₄*C₃₅H₄₁NOPRuS
Molecular Weight:742.631
Hs Code.:

Synonyms:[Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

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Chemical Property of [Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

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Technology Process of [Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

There total 2 articles about [Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 2637-34-5,73018-10-7
2-Sulfanylpyridine

: 178325-73-0
[Ru(η(5)-C5H5)(=C=C=CPh2)(CO)(P(Pr(i))3)](tetrafluoroborate)

: 211561-64-7
[Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

Guidance literature:: In dichloromethane; exclusion of air; equimolar amts., stirring for 5 min; evapn., washing (Et2O); elem. anal.;
DOI:10.1021/om980230a

Reference yield:

: 67969-82-8
tetrafluoroboric acid diethyl ether

: 211561-65-8
[Ru(η(5)-C5H5)(-C(SC5H4N)=C=CPh2)(CO)(P(Pr(i))3)]

: 211561-64-7
[Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

Guidance literature:: In dichloromethane; exclusion of air;
DOI:10.1021/om980230a

Reference yield: 62.0%

: 211561-64-7
[Ru(η(5)-C5H5)(-C=CH-CPh2-NC5H4S)(CO)(P(Pr(i))3)](tetrafluoroborate)

: 211561-65-8
[Ru(η(5)-C5H5)(-C(SC5H4N)=C=CPh2)(CO)(P(Pr(i))3)]

Guidance literature:: With NaOMe; In tetrahydrofuran; byproducts: NaBF4, MeOH; exclusion of air; slight excess of NaOMe, stirring for 2 h; evapn., addn. of MePh, filtration off of NaBF4, evapn., washing (Et2O); elem. anal.;
DOI:10.1021/om980230a