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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67005320HCID 67005320—
SolventEthyl AcetateHCID 8857—
ProductN-(2-Bromo-4-hydroxy-6-methylphenyl)-3-nitrobenzamideHCID 67005440—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067638B2
Source datasetuspto-grants-2011_11
ORD IDord-2057dda266644fa591e9a67f254dd933
Source noteuspto-grants-2011_11