HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (+/-)-3-(Cyclopentyloxy)-4-methoxy-alpha-methylbenzeneacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3-(Cyclopentyloxy)-4-methoxyphenylacetonitrile | HCID 10728228 | — |
| Reactant | Lithium diisopropylamine | HCID 45051747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+/-)-3-(Cyclopentyloxy)-4-methoxy-alpha-methylbenzeneacetonitrile | HCID 22456815 | 100% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A mixture of 3-(cylcopentyloxy)-4-methoxybenzeneacetonitrile (20 g) in THF (200 ml) was stirred at -78° C. under a N2 flow. N-(1-methylethyl)-2-propanamine lithium salt (45 ml) was added dropwise and the resulting mixture was stirred for 30 minutes at -78° C. Iodomethane (13.5 g) was added dropwise and the resulting reaction mixture was allowed to warm to RT. The reaction mixture was stirred for 2 hours. The mixture was quenched with a saturated aqueous NH4Cl solution (200 ml) and was extracted with CH2Cl2 (3×φml). The separated organic layer was dried (MgSO4), filtered and the solvent was evaporated, yielding 17.7 g (100%) of (±)-3-(cyclopentyloxy)-4-methoxy-α-methylbenzeneacetonitrile (interm. 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994376 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-8b78e3eed0174b4fa02bacb28dbd6090 |
| Source note | uspto-grants-1999_11 |