Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Toluene | HCID 1140 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Nitrotoluene | HCID 6944 | — |
| Product | 4-Nitrotoluene | HCID 7473 | — |
Reaction Steps
A 100 mL three-necked reaction flask fitted with reverse dean-stark apparatus was charged with 9.214 g toluene (0.1 mol), 40 mL 1,2 dichloro ethane, and 1.842 g of catalyst as prepared in example 5. The flask was flushed with nitrogen. The reaction mixture was refluxed at 100° 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 reaction 80.5% toluene conversion was obtained with 54.7% selectivity for 2-nitro toluene and 41.6% for 4-nitro toluene. Other products were 3.7%.
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-307a4a1eac894ba787de1301e56da65e |
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| Source note | uspto-grants-2016_08 |
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