HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-[2-(4-Hydroxyphenyl)propan-2-yl]-2-methylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | O-Cresol | HCID 335 | — |
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | p-Isopropenylphenol | HCID 584247 | — |
| Product | 4-[2-(4-Hydroxyphenyl)propan-2-yl]-2-methylphenol | HCID 14389009 | — |
Reaction Steps
Anhydrous HCl was introduced, with adequate cooling, into a mixture of 134 g (1.0 mole) of freshly prepared 4-isopropenylphenol (made by thermally cracking BPA in the presence of catalytic amounts of sodium hydroxide and separating it from the coproduct phenol by fractional vacuum distillation) and 540 g (5.0 moles) of o-cresol, while maintaining the temperature of the ensuing exothermic reaction below 50° C. After 4 hours, the red colored reaction mixture was stripped of HCl and excess cresol under water aspirator vacuum and the resultant straw colored melt was purified by recrystallization from cyclohexane. The 98.7% pure MMEP had a mp of 112°-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04304899 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-105a538dde964662be042e60af7ad9db |
| Source note | uspto-grants-1981_12 |