HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Iodo-3-methyloct-1-en-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Iodooct-1-en-3-one | HCID 53400874 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Iodo-3-methyloct-1-en-3-ol | HCID 54522683 | 86.9% |
Reaction Steps
To a Grignard solution prepared from 1.05 g (0.41 moles) of magnesium and 6.2 g (0.435 moles) of methyl iodide in 30 ml of dry ether under argon is added dropwise 10 g of 1-iodo-1-octen-3-one (Example 183) in 45 ml of ether. The resulting solution is stirred at ambient temperature for one hour. After the addition of 75 ml of saturated ammonium chloride the ether layer is separated and the aqueous layer is separated and the aqueous layer is extracted several times with ether. The combined ether extracts are washed successively with ammonium chloride and water, dried and taken to dryness to give 9.24 g of product as an oil; λ max 2.80, 3.23, 6.24 and 10.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04235797 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-bd4610d327f9413fbb2c658f8ed3e82b |
| Source note | uspto-grants-1980_11 |