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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-4-methylphenol | HCID 7264 | — |
| Reactant | 4-(4-Phenylbutoxy)benzoic Acid | HCID 11043825 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Oxalyl chloride | HCID 65578 | — |
| Product | 2'-Hydroxy-5'-methyl-4-(4-phenylbutoxy)benzanilide | HCID 15106546 | 100.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04994479 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-c0a13a5b193e4057893b9351a46c16b2 |
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| Source note | uspto-grants-1991_02 |
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