HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzenethiol → HCID 67183685, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzenethiol | HCID 7811 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Product | HCID 67183685 | HCID 67183685 | — |
Reaction Steps
The general procedure was used to convert iodobenzene and p-toluenethiol to the title product. Purification by flash chromatography (hexane as the eluent) gave the analytically pure product as a clear oil (388 mg, 97.0% yield). 1H NMR (300 MHz, CDCl3) δ 7.18 (dt, J=8.1, 2H; Ha, Ha′), 7.15–7.12 (m, 4H; He, He′, Hf, Hf′), 7.08 (m, 1H; Hg), 7.04–7.00 (d, J=7.34, 2H; Hc, Hc′), 2.22 (s, 3H; methyl protons). 13C NMR (75 MHz, CDCl3) δ 138.05 (C4), 137.62 (C1′), 132.77 (C2, C6), 131.76 (C1), 130.55 (C3, C5), 130.23 (C2′, C6′), 129.52 (C3′, C5′), 126.87 (C4′), 21.62 (C7). Anal. Calcd. for C13H12S: C, 77.95; H, 6.04; S, 16.01; Found C, 77.78; H, 6.01; S, 16.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112697B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-3429b94c10454299ab4f677ecf2ebdf2 |
| Source note | uspto-grants-2006_09 |