Displacement of THF by dihydrobenzo[b]thiophene (DHBT) in [(triphos)Ir(H)2(THF)]BPh4 yields the h1-SDHBT adduct [(triphos)Ir(H)2(h1-DHBT)]BPh4 which reacts in THF at room temperature with KOBut to give the neutral 2-vinylthiophenolate derivative (triphos)Ir(H)2{h1- o-S(C6H4)CHNCH2} via C2-S bond cleavage; the latter compound is hydrogenated under mild conditions (2 bar H2, 80 °C) to the 2-ethylthiophenolate derivative (triphos)- Ir(H)2{o-S(C6H4)Et} and under harsh conditions (30 bar H2, 160 °C) to free 2-ethylthiophenol and (triphos)IrH3.
First example of opening and hydrogenation of 2,3-dihydrobenzo[b]thiophene to 2-ethylthiophenol assisted by a soluble metal complex
Bianchini C;Meli A;Oberhauser W;Vizza F
1999
Abstract
Displacement of THF by dihydrobenzo[b]thiophene (DHBT) in [(triphos)Ir(H)2(THF)]BPh4 yields the h1-SDHBT adduct [(triphos)Ir(H)2(h1-DHBT)]BPh4 which reacts in THF at room temperature with KOBut to give the neutral 2-vinylthiophenolate derivative (triphos)Ir(H)2{h1- o-S(C6H4)CHNCH2} via C2-S bond cleavage; the latter compound is hydrogenated under mild conditions (2 bar H2, 80 °C) to the 2-ethylthiophenolate derivative (triphos)- Ir(H)2{o-S(C6H4)Et} and under harsh conditions (30 bar H2, 160 °C) to free 2-ethylthiophenol and (triphos)IrH3.File in questo prodotto:
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