HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrafluorophthalonitrile → 2-Phenylpropionitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrafluorophthalonitrile | HCID 74600 | — |
| Reactant | Tetrafluoroisophthalonitrile | HCID 608182 | — |
| Reactant | 2,3,4,6-Tetrafluorobenzonitrile | HCID 22287549 | — |
| Product | 2-Phenylpropionitrile | HCID 15761 | — |
Reaction Steps
By a method similar to Example 11, a reaction was carried out using 2,4,5,6-tetrafluoroisophthalonitrile, instead of 3,4,5,6-tetrafluorophthalonitrile. After 5 hours, the reaction solution was analyzed by gas chromatography, whereupon the conversion of 2,4,5,6-tetrafluoroisophthalonitrile was found to be 36% and the yield of 2,3,4,6-tetrafluorobenzonitrile (based on 2,4,5,6-tetrafluoroisophthalonitrile) was 20%. At the same time, 1.1 mmol of α-methylbenzylcyanide was produced. This corresponded to 0.35 times molar amount relative to the production of 2,3,4,6-tetrafluorobenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020517 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-41e1ed2ba8da46c882cfa7d1e54ed6d9 |
| Source note | uspto-grants-2000_02 |