HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373753Generated: October 29, 2026
Acetonitrile → 3,6-difluoro-4,5-bisphenylthiophthalonitrile
https://huagongshe.com/reaction/373753
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Product | 3,6-difluoro-4,5-bisphenylthiophthalonitrile | HCID 1982243 | — |
Reaction Steps
In a four-neck flask having an inner volume of 200 ml, 19.6 g (98 m.mols) of 3,4,5,6 -tetrafluiorophthalonitrile, 21.6 g (196 m.mols) of thiophenol, 17.1 g (294 m.mols) of potassium fluoride (KF), and 100 ml of acetonitrile were placed and stirred at 50° C. for reaction for 12 hours. Then, the reaction mixture was cooled to room temperature. The yellow solid which formed consequently in the mixture was separated by filtration. The cake thus obtained was purified by washing first with methanol and then with hot water, to obtain 34.5 g of 3,6-difluoro-4,5-bisphenylthiophthalonitrile (yield: 92.5 mol % based on 3,4,5,6-tetrafluoronitrile).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166025 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-fbb790d9103544168132200ae5cedd03 |
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| Source note | uspto-grants-1992_11 |
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