HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916018Generated: October 26, 2026
Dimethylformamide → 2-(Phenylthio)thioxanthone
https://huagongshe.com/reaction/1916018
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chlorothioxanthone | HCID 618848 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Phenylthio)thioxanthone | HCID 66915289 | 45% |
Reaction Steps
Uniformly mixed were 11.0 parts of 2-chlorothioxanthone, 4.9 parts of thiophenol, 2.5 parts of potassium hydroxide, 162 parts of N,N-dimethylformamide, and allowed to react at 130° C. for 9 hours. Subsequently, the reaction solution was cooled to room temperature (about 25° C.) and poured into 200 parts of distilled water, so that the product was precipitated. The product was filtered, and the residue was washed with water until the pH of the filtrate became neutral. Subsequently, the residue was dried under reduced pressure, so that a yellow powdery product was obtained. The product was purified by column chromatography (eluent: toluene/hexane=1/1 in volume ratio) to give 2-(phenylthio)thioxanthone in a yield of 45%. The product was identified by 1H-NMR {d6-dimethylsulfoxide, δ (ppm) 8.43 (1H, d), 8.25 (1H, s), 7.75-7.90 (3H, m), 7.66 (1H, d), 7.60 (1H, t), 7.42-7.46 (5H, m)}.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08617787B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-a07c100ca8ee4a0886c85189012e1b13 |
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| Source note | uspto-grants-2013_12 |
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