HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → alpha-Methyl-p-(2-thenoyl)hydratroponitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-[p-(2-Thenoyl)phenyl]acetonitrile | HCID 12232974 | — |
| Product | alpha-Methyl-p-(2-thenoyl)hydratroponitrile | HCID 21391796 | — |
Reaction Steps
To a stirred mixture of 5.5 parts of sodium hydride dispersion 78% in 150 parts of hexamethylphosphoramide are added dropwise 14 parts of 2-[p-(2-thenoyl)phenyl] acetonitrile over a period of 30 minutes at a temperature of 15° C. Upon completion, stirring is continued for 3 hours at room temperature. Then there are added dropwise 34 parts of methyl iodide (strong exothermic reaction) and upon completion, the whole is stirred overnight. The reaction mixture is poured onto water and the product is extracted three times with 200 parts of benzene. The combined extracts are washed five times with water, dried, filtered and evaporated, yielding α-methyl-p-(2-thenoyl)hydratroponitrile as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04035376 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-4467db2fec654309a1292642c22712dd |
| Source note | uspto-grants-1977_07 |