Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | 5-Dodecyl-2-hydroxybenzoic acid | HCID 19782984 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86744919 | HCID 86744919 | — |
Reaction Steps
To a mixture of 30.6 parts of 5-dodecylsalicylic acid, 21.2 parts of p-xylene, 3.8 parts of 87% paraformaldehyde and 30 parts of acetic acid was added 2.0 parts of 95% sulfuric acid (catalyst). After being heated under reflux for 6 hours, the reaction mixture was washed with water, and unreacted p-xylene and water were removed by vacuum distillation to give 43 parts of 5-dodecylsalicylic acid-p-xylene-formaldehyde co-condensation product. 10 parts of the co-condensation product was added to 32 parts of aqueous 10% potassium hydroxide solution and dissolved at 80° C. The solution was cooled to 40° C., and 28 parts of aqueous 10% solution of nickel chloride hexahydrate was added thereto. After the reaction had been allowed to proceed at 40° C. for 30 minutes, precipitates formed were collected by filtration, washed with water and dried to give 11 parts of nickel salt of 5-dodecylsalicylic acid-p-xylene-formaldehyde co-condensation product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034370 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-f14fa433edf44ebfa000482be78738f7 |
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| Source note | uspto-grants-1991_07 |
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