HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Hydroxyisophthalic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethyl(1-phenylethyl)benzene | HCID 3033855 | — |
| Reactant | HCID 20223815 | HCID 20223815 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Hydroxyisophthalic acid | HCID 69257 | 94.8% |
Reaction Conditions
| Temperature | 280 °C |
|---|
Reaction Steps
Trisodium 5-sulfoisophthalate (312 g) was added to 170 g of a 50% aqueous solution of sodium hydroxide, and the mixture was stirred. Then, 1980 g of 1-phenyl-1-(2,3-dimethylphenyl)-ethane was mixed, and the resulting mixture was heated to 280° C. in a nitrogen stream and dehydrated with stirring. The dehydrated mixture was stirred at 280° C. for 1.5 hours. After cooling, 1 liter of water was added to the reaction mixture to separate the reaction medium. The aqueous layer was decolorized with activated carbon, and precipitated with dilute sulfuric acid to give 172.5 g (yield 94.8%) of 5-hydroxyisophthalic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04633024 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-518834d0c8e6470688cdd7a9923409dc |
| Source note | uspto-grants-1986_12 |