HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480709Generated: October 30, 2026
4-Methylbenzenethiol → HCID 58442533, compound
https://huagongshe.com/reaction/1480709
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylbenzenethiol | HCID 7811 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 58442513 | HCID 58442513 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58442533 | HCID 58442533 | 79% |
Reaction Steps
A mixture of 1-(4-iodo-2,6-dimethylphenyl)ethanone (1.5 g, 5.5 mmol, 1.0 equiv), 4-methylbenzenethiol (1.02 g, 8.2 mmol, 1.5 equiv), copper(I) oxide (39.2 mg, 0.3 mmol, 0.05 equiv), and potassium hydroxide (614.1 mg, 11.0 mmol, 2.0 equiv) in DMF (4.4 mL) and H2O (1.1 mL) was heated at reflux for 20 h. The mixture was quenched with H2O (10 mL) and extracted with ether (2×20 mL). The organic layer was collected, dried over MgSO4(s), and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (3.0% EtOAc in hexanes as eluant) to provide 1-(2,6-dimethyl-4-(p-tolylthio)phenyl)ethanone (1.16 g, 4.3 mmol) as yellow oil in 79% yield: 1H NMR (CD3OD, 500 MHz) δ 7.29 (d, J=8.0 Hz, 2H), 7.20 (d, J=8.0 Hz, 2H), 6.88 (s, 2H), 2.45 (s, 3H), 2.35 (s, 3H), 2.15 (s, 6H); ESI-MS: m/z 271.8 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409902B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4b51eff125a74a1a8ccaee5e4bf270c2 |
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| Source note | uspto-grants-2016_08 |
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