HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086981Generated: November 2, 2026
p-Toluenesulfonic acid → HCID 86744918, compound
https://huagongshe.com/reaction/1086981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | M-Xylene | HCID 7929 | — |
| Reactant | 1,3,5-Trioxane | HCID 8081 | — |
| Reactant | HCID 15745145 | HCID 15745145 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86744918 | HCID 86744918 | — |
Reaction Steps
To a mixture of 26.4 parts of 5-nonylsalicylic acid, 5.9 parts of m-xylene, 3.4 parts of sym-trioxane and 15 parts of acetic acid was added 4.0 parts of p-toluenesulfonic acid (catalyst). After being heated under reflux for 5 hours, the reaction mixture was washed with water, and unreacted m-xylene and water were removed by vacuum distillation to give 38 parts of 5-nonylsalicylic acid-m-xylene-formaldehyde co-condensation product. To 10 parts of the co-condensation product was added gradually a mixture of 0.9 parts of zinc oxide and 0.5 parts of ammonium hydrogencarbonate at a temperature of 150° C. After the completion of the addition, the reaction was allowed to proceed for an additional hour at 150° C. to give 10.8 parts of zinc salt of 5-nonylsalicylic acid-m-xylene-formaldehyde co-condensation product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05034370 |
|---|
| Source dataset | uspto-grants-1991_07 |
|---|
| ORD ID | ord-0c04f199f54741e59064aaf1f62ae2e6 |
|---|
| Source note | uspto-grants-1991_07 |
|---|