HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358586Generated: October 29, 2026
Acetic Anhydride → HCID 178526026, compound
https://huagongshe.com/reaction/358586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178511256 | HCID 178511256 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178526026 | HCID 178526026 | — |
Reaction Steps
A mixture of 2.33 g of trans-4-aminomethyl-1-(4-pyridylcarbamoyl)cyclohexane, 15 ml of 99% formic acid and 18 ml of acetic anhydride was stirred and then an exothermic reaction occurred by 36° C. After refluxing for 10.5 hours, the resultant mixture was poured into ice-water and alkalized with potassium carbonate and an aqueous solution of concentrated sodium hydroxide. To the precipitated water substance was added chloroform. The obtained crystals were collected by filtration, washed with water and dried. The crystals were dissolved in ethanol and a solution of oxalic acid in ethanol added thereto. The precipitated crystals were collected by filtration and dried to give trans-4-formamidomethyl-1-(4-pyridylcarbamoyl)cyclohexane oxalate 1/2 hydrate, melting at 204°-207° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04997834 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-b3380e4023cc4f548555def0c84b6639 |
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| Source note | uspto-grants-1991_03 |
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