Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 2,3-Dichloronitrobenzene | HCID 18555 | — |
| Reactant | Fluoride Ion | HCID 28179 | — |
| Reactant | 4-Methylpentane-1,2-diol | HCID 91171 | — |
| Product | 1-Chloro-2-fluoro-3-nitrobenzene | HCID 75016 | — |
Reaction Steps
In a 1.5 liter flange flask and fitted with a distillation bridge and impeller stirrer, 279 g (4.8 tool) of fluoride, 218.5 g (0.3 mol) of trimethyl(ethoxypolyoxypropyl)ammonium chloride and 11.5 g (0.023 mol) of polyethylene glycol dimethyl ether 500 were introduced at 100° C. into the melt of 768 g (4 mol) of 2,3-dichloronitrobenzene. Subsequently, the mixture was azeotropically dried using 200 g (1.9 mol) of xylene and stirred for 24 hours at a temperature of 100° C. Amount of 3-chloro-2-fluoronitrobenzene formed: after 5 hours: 18 GC area-%. after 24 hours: 47 GC area-%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05492875 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-93715521487843ad811ccacd4c35e9cc |
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| Source note | uspto-grants-1996_02 |
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