Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19813123 | HCID 19813123 | — |
Reaction Steps
A mixture of 4-acetoxybenzoic acid (5.0 g) and triethylamine (3.0 g) in acetone (150 mL) at 0° C. was treated with ethyl chloroformate over 5 minutes with stirring. After a further 10 minutes, sodium azide (21.5 g) in water (10 mL) was added and the mixture maintained at 5° C. for 0.5 hour. The mixture was then concentrated at 45° C. under reduced pressure and the residue dissolved in toluene (200 mL) and washed with water and dried (Na2SO4). After evaporation of 100 mL of the toluene under reduced pressure, the solution was heated under reflux for 1 hour and cooled to 5° C. before addition of n-propylamine (3 mL). After a further 15 minutes, the mixture was evaporated to dryness and the residue dissolved in methanol (50 mL) and warmed with 10% aqueous NaOH (10 mL) at 60° C. for 15 minutes. Evaporation of the methanol and addition of water and 6N HCl gave a solid which was filtered, washed with water and crystallized from acetone-ether to give 4-n-propylaminocarbonylaminophenol (3.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158949 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-3347c298cce04a49a10ef3e1edf63a9f |
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| Source note | uspto-grants-1992_10 |
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