HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178495620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178520919 | HCID 178520919 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178495620 | HCID 178495620 | — |
Reaction Steps
60 ml of THF are added under an N2 atmosphere to 100 mmol of NaH in the form of an oil dispersion. The mixture is mixed vigorously and heated to 45°-50° C. 120 mmol of methyl iodide are then added, and 80 mmol of trans-4-(p-trifluoromethylphenyl)cyclohexylmethyl alcohol in 20 ml of THF are subsequently added dropwise over the course of 30 minutes. The reaction mixture is then stirred for 30 minutes at the same temperature, cooled and carefully hydrolysed using aqueous THF. When the vigorous evolution of H2 is complete, customary work-up gives trans-4-methoxymethyl(p-trifluoromethylphenyl)cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389295 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-3c6dfcfdff6340b4a198e2227e916b33 |
| Source note | uspto-grants-1995_02 |