Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Lithium cyclohexylisopropylamide | HCID 10877271 | — |
| Edukt | Phosphonic acid, 2-furanyl-, diethyl ester | HCID 12485182 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Diethyl 5-iodo-2-furanphosphonate | HCID 22280644 | — |
Reaktionsschritte
A solution of diethyl 2-furanphosphonate (prepared as described in Step A, Example 1) (1 mmol) in 2 mL THF was cooled to −78° C. and added to a solution of lithium isopropylcyclohexylamide (LICA) (1 mmol) in 2 mL THF at −78° C. over 20 min. The resulting mixture was stirred −78° C. for 20 min and added into a solution of iodine (1 mmole) in 1 mL THF at −78° C. over 20 min. The mixture was then stirred at −78° C. for 20 min. Extraction and chromatography provided diethyl 5-iodo-2-furanphosphonate as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06919322B2 |
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| Quelldatensatz | uspto-grants-2005_07 |
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| ORD ID | ord-4dcb8ff61a664596937a2931dd3ade32 |
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| Quellennotiz | uspto-grants-2005_07 |
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