HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthol → 3-Hydroxy-2-naphthoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Nitrilotriacetic Acid | HCID 8758 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tartrazine | HCID 164825 | — |
| Product | 3-Hydroxy-2-naphthoic acid | HCID 7104 | 73% |
Reaction Steps
An autoclave equipped with stirrer is charged with 1,220 parts of β-naphthol, 640 parts of aqueous sodium hydroxide solution (50% strength by weight) and 6 parts of the trisodium salt of nitrilotriacetic acid (dissolved in 15 parts of water). The charge is mixed thoroughly under nitrogen until the internal temperature reaches 260° C. 510 parts of 2-hydroxy-naphthalene-3-carboxylic acid (corresponding to 73% of theory, based on β-naphthol converted) are obtained analogously to Example 1. The proportion of resin formed is 12 mole percent, based on β-naphthol employed. 685 parts of β-naphthol are recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002675 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-de2ea499dc074822814011b821d0fc96 |
| Source note | uspto-grants-1977_01 |