HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 86733776, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl arachidonate | HCID 5367369 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86733776 | HCID 86733776 | — |
Reaction Steps
To a solution of 1.7 g. of n-isopropylcyclohexylamine in 15 ml. of tetrahydrofuran, at -78°, is added 5.5 ml. of a 2.4 N n-butyl lithium n-hexane solution. Then 3 g. of ethyl arachidonate in 150 ml. of tetrahydrofuran is added dropwise, over a 2-hour period, at -78°. Then 1.5 ml. of methyl iodide is added and the mixture is allowed to warm to room temperature. The solution is concentrated by evaporating tetrahydrofuran, then extracted with ether to yield ethyl 2-methylarachidonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03972907 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-c8b4fd74ce794077b094c1624a1e0747 |
| Source note | uspto-grants-1976_08 |