HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052002Generated: October 28, 2026
Carbonic acid-guanidine (1:1) → HCID 86695818, compound
https://huagongshe.com/reaction/1052002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbonic acid-guanidine (1:1) | HCID 286947 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | HCID 86695817 | HCID 86695817 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86695818 | HCID 86695818 | 8.3% |
Reaction Steps
A solution of methyl-4-(3-dimethylaminomethylene-4-oxopiperidin-1-yl)-benzoate (3.00 g, 10.40 mmol) in EtOH (200 mL) was treated with guanidine carbonate (7.50 g, 41.60 mmol), followed by sodium acetate trihydrate (11.32 g, 83.20 mmol). The reaction mixture was refluxed for 16 hours and allowed to cool to room temperature. The insolubles were filtered off and the filtrate was concentrated. The residue was partitioned between water and ethyl acetate and the solid was filtered off, washed with water, ethyl acetate, and dried to give the title compound (258 mg). The filtered insoluble material from the reaction mixture was suspended in water, stirred for 30 minutes, and the remaining light yellow, amorphous solid was collected, washed with water, ethyl acetate, and dried to give an additional amount of the title compound (1.95 g, total yield 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388176B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-e5edc64e2aed472ab786a5fd47a20fcb |
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| Source note | uspto-grants-2016_07 |
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