HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → N-hydroxy-2-methoxy-5-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Benzoic acid, 2-methoxy-5-nitro-, methyl ester | HCID 7020925 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-hydroxy-2-methoxy-5-nitrobenzamide | HCID 57687781 | 101.7% |
Reaction Steps
Methyl 2-methoxy-5-nitrobenzoate (10 g, 47.39 mmol) and hydroxylamine hydrochloride (13.17 g, 189.56 mmol) were taken up in MeOH (100 ml) and a solution of KOH (13.27 g, 236.95 mmol) in MeOH (55 ml) was added carefully. Note—an exothermic reaction was observed; solids initially dissolved, then a solid precipitated out of solution. TLC (run in EtOAc) of an acid washed aliquot showed a trace of the starting benzoate and a new product. H2O (100 ml) was added and any undissolved solid collected by filtration off, washed with isopropyl alcohol (IPA) and dried in vacuo to give 10.23 g (>100%) of N-hydroxy-2-methoxy-5-nitrobenzamide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450506B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-a8c2ccc9ecf741f7b0c5356ef634db92 |
| Source note | uspto-grants-2013_05 |