HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65455Generated: October 29, 2026
Thiophenol → 2,4,5-Trifluoro-6-phenylthioisophthalonitrile
https://huagongshe.com/reaction/65455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Tetrafluoroisophthalonitrile | HCID 608182 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,4,5-Trifluoro-6-phenylthioisophthalonitrile | HCID 13656192 | 63% |
Reaction Steps
A 2.0 g amount of tetrafluoroisophthalonitrile and 0.87 g of potassium fluoride were dissolved in 10 ml of acetonitrile. After cooling the mixture to a temperature of 0° C. by an ice-water bath, 1.1 g of phenyl mercaptan was dropwise added by a syringe. While mixture was maintained at a temperature of about 0° C., the mixture was stirred for 8 hours and the solvent was then distilled off. A 50 ml amount of water was added to the mixture and potassium fluoride was dissolved. The mixture was extracted with chloroform, and the extract was dried with magnesium sulfate. The chloroform was distilled off in vacuo and the resultant liquid was then distilled in vacuo to obtain 1.8 g (63% yield) of the desired compound No. 41 at a boiling point of 65° C. to 67° C./0.7 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04614742 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-e78c1622567544b08df3601068511f5d |
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| Source note | uspto-grants-1986_09 |
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