HuagongsheHuagongshe Chemistry Print Report · For research reference only
Resorcinol → 3-Isopropylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Resorcinol | HCID 5054 | — |
| Reactant | alpha,alpha-Dimethyl-3-(1-methylethyl)benzenemethanol | HCID 26939 | — |
| Reactant | 1-(1-Methylethenyl)-3-(1-methylethyl)benzene | HCID 136907 | — |
| Reactant | 1-(3-(1-Hydroxy-1-methylethyl)phenyl)ethanone | HCID 13531419 | — |
| Reactant | 3-(Prop-1-en-2-yl)phenol | HCID 13536154 | — |
| Reactant | 1-(3-(Prop-1-en-2-yl)phenyl)ethan-1-one | HCID 13574685 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Isopropylphenol | HCID 12059 | — |
Reaction Steps
The reaction mixture formed by the acid-decomposition contains not only resorcin, acetone and the inert solvent used but also various by-products, for example, carbinols such as m-isopropyl-α,α-dimethylbenzyl alcohol, m-acetyl-α,α-dimethylbenzyl alcohol and m-hydroxy-α,α-dimethylbenzyl alcohol, olefins such as m-isopropenylphenol, m-isopropenylacetophenone and m-isopropenylcumene, peroxides which are estimated to have been formed by condensation reaction between carbinols or olefins and hydroperoxides, m-isopropylphenol, m-hydroxyacetophenone, and high-boiling-point condensates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04273623 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-d15bd9b88d374309b04d2b44561763e1 |
| Source note | uspto-grants-1981_06 |