HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458672Generated: November 1, 2026
Hexamethylphosphoramide → HCID 178437721, compound
https://huagongshe.com/reaction/1458672
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Reactant | HCID 178437728 | HCID 178437728 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178437721 | HCID 178437721 | — |
Reaction Steps
8.4 g of trifluoromethyl iodide and 5 g of copper powder were stirred with 20 ml of hexamethylphosphoric triamide in a stainless steel laboratory autoclave (Hastelloy) at 120° C. for 2.5 hours. The mixture was filtered with suction over Celite, under nitrogen, to remove the excess copper powder. 1.92 g (5 mmol) of 4-(cis-4-tert-butyl-cyclohexylamino)-6-ethyl-5-iodopyrimidine (Example 1) were added in order to dissolve the trifluoromethyl-copper complex, and the mixture was stirred under nitrogen at 100° C. for 2 hours. After cooling, 200 ml of diethyl ether were added, the precipitated copper salts were filtered off and the filtrate was extracted by stirring with water. The organic phase was dried and concentrated. The product was purified by filtration over a silica gel column (petroleum ether/ethyl acetate 7:3) to give 0.52 g (32% of theory) of product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05852023 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-253942af0fa34b9e9c4c7e915be29e0d |
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| Source note | uspto-grants-1998_12 |
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