HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-nitrobenzene → p-Fluoronitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Catalyst | HCID 13306852 | HCID 13306852 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | p-Fluoronitrobenzene | HCID 9590 | 96.3% |
Reaction Steps
A reaction mixture of 85.3 g of 4-chloronitrobenzene (CNB), 45.3 g of potassium fluoride, 1.4 g of the N-neopentyl-4-(N',-N'-di-n-butylamino)pyridinium chloride (NPDBAPC) obtained in Example lII in 109.6 g of sulfolane was heated with stirring for 9 hours at 205°-215° C. At the end of this period, HPLC assay of a sample of the reaction mixture indicated less than 1% residual CNB. Simple distillation of the reaction mixture under vacuum gave 73.6 g of 4-fluoronitrobenzene (FNB) for a 96.3% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973772 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-aeaf7bb70e374d6e8e8a31961025304d |
| Source note | uspto-grants-1990_11 |