HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895566Generated: October 26, 2026
Phenethylthiophenol → HCID 178420258, compound
https://huagongshe.com/reaction/1895566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethylthiophenol | HCID 67226359 | — |
| Reactant | HCID 178521537 | HCID 178521537 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178420258 | HCID 178420258 | 71% |
Reaction Steps
To a mixture of trans-6,13-dihydroxy-6,13-dihydropentacene (1.0 g, 3.20 mmol) and zinc iodide (1.02 g, 3.20 mmol) were added successively dry CH2Cl2 (100 mL) and phenethylthiophenol (0.77 g, 7.03 mmol) at RT under an argon atmosphere. The resulting mixture was stirred at RT for 2 h, and then quenched with H2O. The mixture was extracted with CH2Cl2, and the organic layer was washed with brine and dried over anhyd. Na2SO4. After evaporation of solvents, the residue was purified by column chromatography on silica gel eluted with n-hexanes-CH2Cl2 (2:1) to give product as white solids in 71% yield (1.13 g). 1H NMR (500 MHz, CDCl3): δ 7.80 (m, 4H), 7.70 (s, 4H), 7.46 (m, 4H), 7.29 (t, 4H, J=7.56 Hz), 7.20 (m, 6H), 5.24 (s, 2H), 2.90 (s, 8H). LDI-MS m/z: 552 [M+], 416 [M+-SCH2CH2C6H5], 280 [M+-2(SCH2CH2C6H5)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513466B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-75465c89ac2d436ea923bb5810711ca3 |
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| Source note | uspto-grants-2013_08 |
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