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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982217Generated: October 31, 2026

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

https://huagongshe.com/reaction/982217

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994479
Source datasetuspto-grants-1991_02
ORD IDord-c0a13a5b193e4057893b9351a46c16b2
Source noteuspto-grants-1991_02