Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Octyloxy)benzoic acid | HCID 17231 | — |
| Solvent | Triphenyl phosphite | HCID 7540 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 19094847 | HCID 19094847 | — |
Reaction Steps
A 500 ml 3-neck round bottom flask containing a magnetic stirrer, thermometer, and a reflux condensor with a gas egress tube for a nitrogen blanket is charged with a one part apiece of p-(n-octyloxy)benzoic acid and urea dissolved in 15 parts N-methylpyrrolidone containing 0.01wt percent triphenylphosphite. The mixture is heated to 120 deg C. for approximately 2-5 hours and then cooled. The addition of a copious amount of 3M aqueous sodium hydroxide to a cooled solution precipitates the product, which is isolated by filtration. Infrared absorbance at 3250 cm-1 (urea N--H stretching) and at 1705 cm-1 and 1640 cm-1 (amide and urea C=O stretching, respectively) in addition to the conspicuous absence of any absorbance at 3490 cm-1 (acid O--H stretching) confirm the chemical transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292351 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-ff9408c4f1f64d81bc2b440859e6597b |
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| Source note | uspto-grants-1994_03 |
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