HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 136117602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Nitrosylsulfuric acid | HCID 82157 | — |
| Reactant | 2,4-Dicyanoaniline | HCID 88169 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 136117602 | HCID 136117602 | 244.3% |
Reaction Steps
20.7 g 2,4-dicyanoaniline were diazotised with 48 g nitrosylsulphuric acid at 0 to 5° C. in a solution comprising 200 ml glacial acetic acid, 40 ml of 85% phosphoric acid and 7.5 ml of concentrated aqueous sulphuric acid, and the batch was subsequently stirred for 1 hour. The reaction mixture was slowly added to a solution of 16 g phenol and 3 g urea in 120 ml water, the temperature being held at 10° C. and the pH being maintained at 6.3-6.5 with caustic soda solution. After stirring for a further 1 hour, the precipitate was filtered off under suction, washed with water, dried, and recrystallised from toluene. 30.3 g of orange-red 4-hydroxy-2′,4′-dicyano-azobenzene were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441113B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-83ed25c2403b4c14842c11ebfdb45f54 |
| Source note | uspto-grants-2002_08 |