HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → 2-Cyano-4-nitrobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Ammonium nitrate | HCID 22985 | — |
| Reactant | (1,1'-Biphenyl)-2-carbonitrile | HCID 141162 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Cyano-4-nitrobiphenyl | HCID 21468957 | 94.4% |
Reaction Steps
2-Cyanobiphenyl (0.111 moles, 20.0 g) and ammonium nitrate (10.0 grams) were added to 250 ml chloroform. Trifluoroacetic anhydride (80 ml) was added. The reaction mixture was stirred until the ammonium nitrate was dissolved. The reaction mixture was added to 300 ml of ice water. The organic layer was separated, dried over sodium sulfate, and concentrated in vacuo to yield 23.5 g of 2-Cyano-4-nitrobiphenyl. (MS)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05612360 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-289cc3603f384c688a4e5d086f0350f0 |
| Source note | uspto-grants-1997_03 |