Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | HCID 23673220 | HCID 23673220 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 5370806 | HCID 5370806 | 71.8% |
Reaction Steps
64.7 g (0.43 mol) of 2-nitrobenzaldehyde and 105.7 g (0.43 mol) of 4-bromophenylacetic acid sodium salt are dissolved in 500 ml of acetic anhydride and stirred at 80° C. for 2 h. When the reaction is complete, the mixture is extended with 1000 ml of water and 750 ml of EtOH and heated to 110° C., and, after 20 min, the orange solid is filtered off with suction, washed with water and MeOH and dried, giving 107 g (71.8%) of a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993123B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9ebea307b4e347a5940025823d6a295e |
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| Source note | uspto-grants-2015_03 |
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