HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 57384643, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 67973124 | HCID 67973124 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 57384643 | HCID 57384643 | — |
Reaction Steps
To sodium [123I] iodide, received in 5-20 μL 0.05M sodium hydroxide is added ammonium acetate buffer (100 μL pH 4.0, 0.2M), sodium [127I] iodide (10 μL, 1 mM solution in 0.01M sodium hydroxide, 1×10−8 moles), peracetic acid (PAA) solution (10 μL 1 mM solution, 1×10−8 moles) and finally 10-(5-tributylstannyl-isoxazol-3-yl)-decanoic acid solution in ethanol or acetonitrile (53 μg, 1×10−7 moles). The reaction mixture is allowed to stand at room temperature for 15 minutes and the iodinated product 10-(4-iodo-[1,2,3]triazol-1-yl)-decanoic acid purified by HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09138493B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-3e1936dbf9bd4930a437b7a446273b7e |
| Source note | uspto-grants-2015_09 |