HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adipic Acid → HCID 86746458, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adipic Acid | HCID 196 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 227803 | HCID 227803 | — |
| Reactant | Oleyl Alcohol | HCID 5284499 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86746458 | HCID 86746458 | — |
Reaction Steps
Seventeen millimoles of tetradecenylsuccinic anhydride (5.0 gm), 34 millimoles of oleyl alcohol (9.1 gm), 50 mg of adipic acid and 10 ml of toluene were combined in a boiling flask (with attached Dean-Stark trap) and refluxed for about 6 hours in the presence of the catalyst p-toluenesulfonic acid. Excess toluene was removed at ambient pressure. The residue was applied to a silica gel column, and eluted with petroleum ether. Elution with petroleum ether gave dioleyl tetradecenylsuccinate. Oleyl alcohol and other impurities were retained on the column. The dioleyl tetradecenylsuccinate has a low melting point and can be used for the commercial production of calorie-reduced fried snack foods.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05176933 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-c6e969a2a18d4b858c7481d305f13df8 |
| Source note | uspto-grants-1993_01 |