HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Iodotoluene → Sulfide, butyl o-tolyl
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Iodotoluene | HCID 5128 | — |
| Edukt | Dibutyl sulfide | HCID 11002 | — |
| Produkt | Sulfide, butyl o-tolyl | HCID 580217 | — |
Reaktionsschritte
The general procedure was used to convert 2-iodotoluene and n-butyl sulfide to the title product. Purification by flash chromatography (hexane as the eluent) gave the analytically pure product as a clear oil (331 mg, 93% yield). 1H NMR (300 MHz, CDCl3) δ 7.17–6.97 (m, 4H; Ha, Hb, Hc, Hd), 2.80–2.78 (t, J=7.3, 2H; Hf), 2.27 (s, 3H; He), 1.61–1.51 (m, 2H; Hg,), 1.44–1.17 (m, 2H; Hh), 0.87–0.82 (t, J=7.3, 3H; methyl protons). 13C NMR (75 MHz, CDCl3) δ 137 (C1), 136.3 (C6), 129.9 (C5), 127.1 (C2), 126.2 (C3), 125.1 (C4), 32.3 (C8), 31 (C9), 22 (C10), 20.2 (C7), 13.6 (C11). Anal. Calcd. for C11H16S: C, 73.27; H, 8.94; S, 17.78; Found C, 73.23; H, 9.16, S, 17.57.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07112697B1 |
| Quelldatensatz | uspto-grants-2006_09 |
| ORD ID | ord-55b990dd3cf640209c06d7df3796034a |
| Quellennotiz | uspto-grants-2006_09 |