HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680981Generated: November 1, 2026
Hydrochloric Acid → HCID 135702827, compound
https://huagongshe.com/reaction/1680981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Heptylaniline | HCID 142169 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 135702827 | HCID 135702827 | 71% |
Reaction Steps
32.9 g (0.17 M) of 4-heptylaniline was cooled to 0° C. or below, 85 g of 10% aqueous hydrochloric acid solution was added, and then a solution of 12.1 g of sodium nitrite in 70 ml of water was added. During the addition, the mixture was cooled so as not to exceed 0° C. After the addition, the mixture was allowed to react for 30 minutes, transferred into a dropping funnel and added dropwise into 300 ml of an 8% NaOH aqueous solution containing 16 g of phenol held at 5° C. or below. After the addition, the mixture was stirred for 1 hour, and then 10% hydrochloric acid aqueous solution was added thereto until a pH of 5-6 to precipitate the reaction product. The precipitate was separated by filtration, washed with water and dried overnight under reduced pressure. After the drying, the product was washed with 500 ml of petroleum ether and further dried under reduced pressure to obtain 34.7 g (0.12 M) of 4-hydroxy-4'-heptylazobenzene. The yield was 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05167857 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-5e354ccad55643a3ac575fa316947654 |
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| Source note | uspto-grants-1992_12 |
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