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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895566Generated: October 26, 2026

Phenethylthiophenol → HCID 178420258, compound

https://huagongshe.com/reaction/1895566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylthiophenolHCID 67226359—
ReactantHCID 178521537HCID 178521537—
Catalystzinc(II)iodideHCID 9883512—
SolventDichloromethaneHCID 6344—
ProductHCID 178420258HCID 17842025871%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513466B2
Source datasetuspto-grants-2013_08
ORD IDord-75465c89ac2d436ea923bb5810711ca3
Source noteuspto-grants-2013_08