HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456902Generated: October 29, 2026
Dicyclohexylcarbodiimide → Desethyl-N-acetylprocainamide
https://huagongshe.com/reaction/1456902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | p-Acetamidobenzoic acid | HCID 19266 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Desethyl-N-acetylprocainamide | HCID 155689 | — |
Reaction Steps
Desethyl-N-acetylprocainamide was prepared by dissolving 1.0 g of p-acetamidobenzoic acid and 0.7 g N-hydroxysuccinimide in 20 ml pyridine. To this solution was added 1.4 g of N,N'-dicyclohexylcarbodiimide. The reaction mixture was placed at 4° C. for 18 hours, at which time the crystals were removed by filtration. The filtration was brought to room temperature and with stirring, 0.51 g N-ethylethylenediamine ethylethylenediamine was added. Stirring continued for 3 hours, the solution was cooled to 4° C. and allowed to react for an addition 24 hours at 4° C. The second crop of crystals was removed by filtration, dissolved in 25 ml of distilled water. The pH was adjusted to 10 with sodium hydroxide to form a white precipitate of desethyl-N-acetylprocainamide. The resultant precipitate was dried in vacuo and stored at -20° C. in a desiccator.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05846703 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-524267702cba4f42a4284ce17ea11779 |
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| Source note | uspto-grants-1998_12 |
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