HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118637Generated: November 1, 2026
Potassium Carbonate → HCID 178477246, compound
https://huagongshe.com/reaction/2118637
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86741669 | HCID 86741669 | — |
| Reactant | HCID 131715218 | HCID 131715218 | — |
| Catalyst | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178477246 | HCID 178477246 | 180% |
Reaction Steps
Then, 30 ml of an aqueous solution containing 3.2 g (10 mmol) of the above-obtained 2-selenoisourea malic acid hydrobromide was prepared. To the solution was dropwise added 20 ml of an aqueous potassium carbonate solution containing 2.04 g (22 mmol) of potassium carbonate at -10° C. To the thus obtained solution was dropwise added 3.51 g (10 mmol) of triethylphosphine gold chloride dissolved in ethanol containing a few drops of methylene chloride at -10° C., and then the mixture was stirred for 30 minutes while cooling, thereby to precipitate crystals. The crystals were filtered off and washed with water-ethanol, 0.1 N HCl and water, successively, thereby to obtain 3 g (6 mmol) of triethylphosphine gold selenomalate. The thus obtained triethylphosphine gold selenomalate was suspended in 20 ml of an aqueous solution containing 320 mg (3 mmol) of Na2CO3. The suspension was stirred for one hour and subjected to lyophilization. Thus, there was obtained 3 mmol of triethylphosphine gold sodium selenomalate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04680286 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-353b1fc4cb4049068210a2e05b921720 |
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| Source note | uspto-grants-1987_07 |
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