HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloro-4-nitrobenzene → 2-Chloro-1-fluoro-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloro-4-nitrobenzene | HCID 7443 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Catalyst | O-Xylene | HCID 7237 | — |
| Product | 2-Chloro-1-fluoro-4-nitrobenzene | HCID 67688 | 71% |
Reaction Steps
In a 1-liter flange flask fitted with a distillation bridge and impeller stirrer, 240 g (4.1 mol) of potassium fluoride, 30 g (0.05 mol) of dimethyldi (ethoxypolyoxypropyl methyl ether)ammonium chloride and 30 g of xylene were introduced at 70° C. into the melt of 767 g (4.0 mol) of 3,4-dichloronitrobenzene, and the reaction suspension was azeotropically dried under reduced pressure up to 120° C. 498 g (2.84 mol) of 3-chloro-4-fluoronitrobenzene were isolated. Amount of 3-chloro-4-fluoronitrobenzene formed, according to GC analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476976 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-6080ea679795486bbaedbe920afdff5f |
| Source note | uspto-grants-1995_12 |