HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758585Generated: November 2, 2026
Phenol → Phenol, 4-[1-(4-aminophenyl)-1-methylethyl]-
https://huagongshe.com/reaction/1758585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | p-Isopropenylphenol | HCID 584247 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Catalyst | Bisphenol A | HCID 6623 | — |
| Product | Phenol, 4-[1-(4-aminophenyl)-1-methylethyl]- | HCID 11148864 | 378.5% |
Reaction Steps
Ten grams of aniline was added to a mixture consisting of 13.0 g of phenol, 3.4 g of p-isopropenyl phenol monomer, 8.5 g of a linear dimer of p-isopropenyl phenol, 1.1 g of a linear trimer of p-isopropenyl phenol and 0.8 g of a linear tetramer and higher polymers of p-isopropenyl phenol (1.05 mole of aniline per mole of the p-isopropenyl phenol monomeric unit). The mixture was stirred at 180° C. Then, 0.2 g of 10% hydrochloric acid (0.0053 mole per mole of the p-isopropenyl phenol monomeric unit) was added, and the reaction was performed for 2 hours. Gas-chromatographic analysis of the reaction mixture showed that 0.38 g of bisphenol A and 21.8 g (yield 93%) of 2-(4'-hydroxyphenyl)-2-(4'-aminophenyl)-propane were formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04374272 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-6d9aeae834bd4baaa4db52a744edef25 |
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| Source note | uspto-grants-1983_02 |
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