HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Hydroxyisophthalonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 4-Methoxybenzene-1,3-dicarbonitrile | HCID 5061995 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Product | 4-Hydroxyisophthalonitrile | HCID 12325963 | 61% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
4-Methoxyisophthalonitrile (2 g, 0.12 mol; see step (ii) above) was dissolved in quinoline (20 mL) and TMSI (2.7 mL, 0.018 mol) was added. The reaction mixture was stirred at 120° C. for 14 h, before being cooled to RT, acidified with conc. HCl and extracted with ethyl acetate. The organic layer was washed with 10% aqueous NaOH and the aqueous layer was acidified with 1 N HCl. The product was extracted with ethyl acetate, washed with water and brine and dried over Na2SO4. Solvent evaporation under reduced pressure afforded the sub-title compound (1.1 g, 61%) as pale brown solid. This was employed directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928225B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-e840436863ab4267af99fd746a269c03 |
| Source note | uspto-grants-2011_04 |