HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 86733027, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Phosphonium iodide ((PH4)I) | HCID 166618 | — |
| Reactant | HCID 86733029 | HCID 86733029 | — |
| Reactant | HCID 86733031 | HCID 86733031 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86733027 | HCID 86733027 | — |
Reaction Steps
1.51 g (3.0 mmol) of finely powdered (4-ethylenedioxybutyl)-triphenyl-phosphonium iodide are suspended in 10 ml of tetrahydrofuran and treated dropwise with a solution of 4.5 mmol of butyl-lithium in hexane. The solution, turns red as the phosphonium iodide goes into solution as (4-ethylenedioxy-butylidene)-triphenyl-phosphorane. After approximately 10 minutes, 0.25 ml (4.5 mmol) of methyl iodide are added to this solution, which thereby becomes lighter, and the (4-ethylenedioxy-1-methylbutyl)-triphenyl-phosphonium iodide which is formed partially precipitates as an oil. After 10 minutes, 3.0 mmol of butyl-lithium in hexane are added dropwise and the solution thereby again becomes dark red.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962283 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-f4b02dcc377346ee852c8eb6b7ddcd00 |
| Source note | uspto-grants-1976_06 |