Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Solvent | Water | HCID 962 | — |
| Product | Nitrobenzene | HCID 7416 | — |
Reaction Steps
A 100 mL three-necked reaction flask fitted with reverse dean-stark apparatus was charged with 7.8 g benzene (0.1 mol), 60 mL 1,2 dichloro ethane, and 1.56 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 6.42 mL (0.1 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 18.6% benzene conversion was obtained with 100% selectivity for mono nitro benzene.
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-decd51250ee940139b25270c0f81a909 |
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| Source note | uspto-grants-2016_08 |
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