Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Phenol | HCID 996 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Nitrophenol | HCID 980 | 46.5% |
| Product | Phenol | HCID 996 | 100% |
| Product | 2-Nitrophenol | HCID 6947 | 46.5% |
Reaction Steps
A 100 mL three-necked round bottom flask fitted with reverse dean-stark apparatus was charged with 9.411 g (0.1 mol) phenol, 60 mL 1,2 dichloro ethane and 1.882 g of catalyst as prepared in example 5. The reaction flask was flushed with nitrogen. The reaction mixture was refluxed at 110° C. for 1 h followed by dropwise addition of 8.6 mL (0.133 mol) of 70% HNO3. The water formed during the reaction was removed using reverse dean-stark apparatus. The reaction was carried out for 8 h. The reaction was monitored by GC analysis. In this case, 100% phenol conversion was obtained with 46.5% 2-nitro phenol and 46.5% 4-nitro phenol. Other unidentified products were 7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409854B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-44873f563b9b4e38836fe210ed944f9f |
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| Source note | uspto-grants-2016_08 |
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