HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793763Generated: November 2, 2026
Hydrochloric Acid → HCID 135677702, compound
https://huagongshe.com/reaction/1793763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Nitrosylsulfuric acid | HCID 82157 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 135677702 | HCID 135677702 | — |
Reaction Steps
18.8 g 4-cyanoaniline are heated at 60° C. in 100 ml water. To dissolve the solid, 10 ml conc. hydrochloric acid are added. A further 115 ml hydrochloric acid are then added, the temperature of the solution is brought to 0° C., 52 g nitrosylsulfuric acid are slowly added dropwise and the mixture is stirred for 1 h. This solution is slowly added dropwise to a solution of 27.5 g 2-bromophenol, 100 ml methanol and 100 ml water at 10° C. A pH of 6–6.5 is maintained by simultaneous addition of 10% sodium hydroxide solution. When the addition is complete, the stirred mass is allowed to react for a further hour and the precipitate is filtered off with suction. The product is then washed with water and dried. The yield of 4-hydroxy-3-bromo-4′-cyanoazobenzene is 68 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07022460B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-0c559d4984104c8aaaba634ab0fdd6b6 |
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| Source note | uspto-grants-2006_04 |
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