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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847278Generated: October 31, 2026

2-Amino-4-methylphenol → 2'-Hydroxy-5'-methyl-4-(4-phenylbutoxy)benzanilide

https://huagongshe.com/reaction/847278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylphenolHCID 7264—
Reactant4-(4-Phenylbutoxy)benzoic AcidHCID 11043825—
CatalystDimethylformamideHCID 6228—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventOxalyl chlorideHCID 65578—
Product2'-Hydroxy-5'-methyl-4-(4-phenylbutoxy)benzanilideHCID 15106546100.8%

Reaction Steps

One drop of N,N-dimethylformamide was added to a solution of 1 g of p-(4-phenylbutoxy)benzoic acid in 5 ml of methylene chloride and 2 ml of oxalyl chloride was added to the mixture at -30° C. or lower. The mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure to obtain crude p-(4-phenylbutoxy)benzoyl chloride. This substance was dissolved in 5 ml of methylene chloride and the resulting solution was added to a solution of 1 g of 2-amino-4-methylphenol in 5 ml of pyridine under ice cooling followed by stirring at room temperature for 3 hours. The reaction mixture was poured into conc. hydrochloric acid-ice and then extracted with ethyl acetate. The extract was washed subsequently with water, an aqueous solution of sodium hydrogen carbonate and again water. After drying over anhydrous magnesium sulfate, the system was concentrated under reduced pressure to obtain 1.4 g of 2'-hydroxy-5'-methyl-4-(4-phenylbutoxy)benzanilide. Melting point: 138°~140 ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140046
Source datasetuspto-grants-1992_08
ORD IDord-6e6167f2e9b54cc987d2459697599245
Source noteuspto-grants-1992_08