HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564293Generated: October 29, 2026
Methanol → N-(2-Bromo-4-hydroxy-6-methylphenyl)-3-nitrobenzamide
https://huagongshe.com/reaction/564293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67005320 | HCID 67005320 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-Bromo-4-hydroxy-6-methylphenyl)-3-nitrobenzamide | HCID 67005440 | — |
Reaction Steps
N-(2-bromo-6-methyl-4-pivaloyloxyphenyl) 3-nitrobenzamide and an aqueous solution of sodium hydroxide were added to methanol, and the resulting mixture was stirred at 70° C. for 3 hours. The solvent was removed under a reduced pressure to obtain a residue. The resulting residue was dissolved in ethyl acetate, washed with aqueous 2N hydrochloric acid solution, and then dried over anhydrous magnesium sulfate. The solvent was removed under a reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:EtOAc=1:1) to obtain N-(2-bromo-6-methyl-4-hydroxyphenyl) 3-nitrobenzamide. Then, the desired title product was prepared according to the conditions as described in Example 1-3 (Yield: 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067638B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-2057dda266644fa591e9a67f254dd933 |
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| Source note | uspto-grants-2011_11 |
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