HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → [1-Cyano-2-(tetrahydro-pyran-4-yl)-hex-5-enyl]-phosphonic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | [1-Cyano-2-(tetrahydro-pyran-4-yl)-vinyl]-phosphonic acid diethyl ester | HCID 72481733 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [1-Cyano-2-(tetrahydro-pyran-4-yl)-hex-5-enyl]-phosphonic acid diethyl ester | HCID 59428163 | — |
Reaction Steps
In a flask, Mg (5.7 g) was placed in THF (50 mL) with an iodine chip. The reaction mixture was vigorously stirred and heated slightly, as 4-bromobutene (25 mL) was added. After consumption of Mg metal, the resulting solution was cannulated into a flask containing a mixture of [1-cyano-2-(tetrahydro-pyran-4-yl)-vinyl]-phosphonic acid diethyl ester (21.78 g, 79.7 mmol), prepared as described in Example 1 Step D above, and CuI (0.3 g) with THF (30 mL). The resulting mixture was stirred for three hours. Saturated aqueous NH4Cl solution and ethyl acetate were then added. The organic layer was separated and dried with MgSO4, filtered, and evaporated in vacuo to yield an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786116B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-683559c8c93d46d3a973bd7f23790b4f |
| Source note | uspto-grants-2010_08 |