HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 86648183, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | tert-Butyl [(4-cyanocyclohexyl)methyl]carbamate | HCID 27281767 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86648183 | HCID 86648183 | — |
Reaction Steps
To a cooled (−78° C.) solution of tert-butyl (4-cyanocyclohexyl)methylcarbamate (500 mg) in tetrahydrofuran (10 mL) was added lithium diisopropylamide (2.0 mL, 2M in heptane). The mixture was stirred at −78° C. for 30 minutes before the addition of CH3I (1 mL). The mixture was then stirred and the temperature was allowed to warm to room temperature. The reaction was quenched with aqueous NH4Cl and the mixture was extracted with ethyl acetate (300 mL) and washed with water, brine and dried over Na2SO4. Filtration and evaporation of the solvent and silica gel chromatography (40% ethyl acetate in hexane) of the crude material gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045475B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-bef82ee2d1c14b4bb9bb881effe9e6a2 |
| Source note | uspto-grants-2015_06 |