Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Hexylaniline | HCID 36382 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 33228-49-8 | HCID 135702828 | 62.3% |
Reaction Steps
30.1 g (0.17M) of 4-hexylaniline was cooled below 0° C. and 85 g of 10% aqueous hydrochloric acid solution was added thereto. To the mixture was then added dropwise an aqueous solution of 11.6 g of sodium nitrite in 68 g of water while cooling the mixture so as not to exceed 0° C. After the dropwise addition, the reaction was continued for 30 minutes. The reaction mixture was transferred into a dropping funnel and added dropwise therefrom into 170 g of an 8%-NaOH aqueous solution containing 16 g of phenol while the temperature was kept below 5° C. After the dropwise addition, stirring was continued for 0.5 hour, and thereafter a 10% aqueous hydrochloric acid solution was added until the pH reached 5-6 thereby precipitating the reaction product. The precipitate was separated by filtration, washed with water and dried under reduced pressure overnight. The dried product was washed with 500 ml of petroleum ether and dried under reduced pressure to obtain 29.6 g (0.10M) of 4-hydroxy-4'-hexylazobenzene The yield was 59%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04979805 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-199357a06ed741be9eaa36eb0292a7ab |
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| Source note | uspto-grants-1990_12 |
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