HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → Diphenyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Product | Diphenyl sulfide | HCID 8766 | — |
Reaction Steps
The general procedure was used to convert iodobenzene and thiophenol to the title product. Purification by flash chromatography (hexane as the eluent) gave the analytically pure product as a clear oil (360 mg, 98% yield). 1H NMR (300 MHz, CDCl3) δ 7.48–7.44 (m, 4H; Ha, Ha′, Hd, Hd′), 7.42–7.39 (m, 4H; Hb, Hb′, He, He′), 7.37–7.31 (m, 2H; Hc, Hc′). 13C NMR (75 MHz, CDCl3) δ 135.70 (C1), 130.94 (C2), 129.10 (C3), 126.94 (C4). Anal. Calcd. for C12H10S: C, 77.37; H, 5.41; S, 17.21; Found C, 77.50; H, 5.45; S, 17.00.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112697B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-43af12036d7d48708a45a49fb2548890 |
| Source note | uspto-grants-2006_09 |