4-Aminophenol → HCID 23273556, compound

To a solution of 22 g of p-aminophenol in 100 ml of acetonitrile was slowly added dropwise 26 ml of phenyl chloroformate under ice-cooling, and the mixture was stirred at room temperature for 2 hours. To the mixture was added 17 ml of pyridine at room temperature, followed by stirring for 1 hour. After completion of the reaction, the reaction solution was poured into 1 l of ice-water to precipitate white crystals. The crystals were collected by filtration, washed twice with 50 ml of water, and dried to obtain 6 g of phenyl 4-hydroxycarbanilide. Subsequently, the crystals were slowly added to a solution of 62 g of hydrazine hydrate (80%) in 50 ml of methanol under ice-cooling, followed by stirring at room temperature for 3 hours. The reaction solution was poured into 1 l of ice-water to precipitate white crystals. The thus formed crystals were collected by filtration, washed once with 20 ml of water and then twice with 50 ml of isopropyl alcohol, and dried to obtain 15 g of 4-(4-hydroxyphenyl)semicarbazide (melting point: 184-186° C.).

1. temperaturecooling
2. stirringby stirring for 1 hour
3. customAfter completion of the reaction
4. customto precipitate white crystals
5. filtrationThe crystals were collected by filtration
6. washwashed twice with 50 ml of water
7. customdried
8. customto obtain 6 g of phenyl 4-hydroxycarbanilide
9. temperaturecooling
10. stirringby stirring at room temperature for 3 hours
11. customto precipitate white crystals
12. filtrationThe thus formed crystals were collected by filtration
13. washwashed once with 20 ml of water
14. dry with materialtwice with 50 ml of isopropyl alcohol, and dried

ORD record

ord-3117b0630bfa400ea51e8796e6c3e9f3

Source dataset

uspto-grants-1991_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05064751