HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118639Generated: October 29, 2026
2-Bromo-N-phenylacetamide → HCID 178419726, compound
https://huagongshe.com/reaction/2118639
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-N-phenylacetamide | HCID 94818 | — |
| Reactant | HCID 178513448 | HCID 178513448 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178419726 | HCID 178419726 | — |
Reaction Steps
6.4 g of phenylcarbamoylmethyl bromide and 3.7 g of selenourea were boiled in 100 ml of acetone under reflux for one four. Then, the mixture was cooled, thereby to form a precipitate. The precipitate was filtered off to obtain phenylcarbamoylmethyl selenoisourea hydrobromide ##STR14## Then, 30 ml of an aqueous solution containing 3.4 g (10 mmol) of the above-obtained phenylcarbamoylmethyl selenoisourea hydrobromide was prepared. To the thus obtained solution was dropwise added 20 ml of an aqueous potassium carbonate solution containing 1.66 g (12 mmol) of potassium carbonate at -10° C. To the 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 one hour at -10° C. to precipitate crystals. The crystals were filtered off, washed with water-ethanol and water, successively, and dried. Thus, there was obtained 2.9 g (5.5 mmol) of [(phenylcarbamoyl) methyl]seleno (triethylphosphine) gold.
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-655aba65cd3542459268995b69a32f46 |
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| Source note | uspto-grants-1987_07 |
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