HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620343Generated: October 26, 2026
Hydrochloric Acid → Phenol, 4-[1-(4-aminophenyl)-1-methylethyl]-
https://huagongshe.com/reaction/620343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | p-Isopropenylphenol | HCID 584247 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenol, 4-[1-(4-aminophenyl)-1-methylethyl]- | HCID 11148864 | — |
Reaction Steps
A mixture of 134.0 grams (1.0 mole) of p-isopropenylphenol and 186.0 grams (2.0 moles) of aniline was stirred and heated to 150° C. To the mixture was added 5.0 grams of a solution obtained by adding 1.28 grams of 10% hydrochloric acid to 93 grams of aniline and stirring the mixture well. The reaction was carried out for 3.0 hours (10,800 s) at the 150° C. reaction temperature. The reaction product was cooled to 120° C. then 350 milliliters of toluene was added. The product was then cooled to 25° C. and the solid precipitated product was recovered by filtration. The crude product was slurried into 350 milliliters of methanol and heated to a reflux then maintained for 15 minutes (900 s). After cooling, the product was recovered by filtration and dried under vacuum to yield 4-(1-(4-aminophenyl)-1-methylethyl)phenol as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820798 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-53e4024461c343c4bb1dd5a73b54f312 |
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| Source note | uspto-grants-1989_04 |
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