HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-(3-(2,6-Dimethylbenzyloxy)phenyl)-2-methylpropanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (2,6-Dimethylphenyl)methanol | HCID 186748 | — |
| Reactant | 2-(3-Hydroxyphenyl)-2-methylpropanenitrile | HCID 12538155 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-(2,6-Dimethylbenzyloxy)phenyl)-2-methylpropanenitrile | HCID 66875329 | — |
Reaction Steps
A solution of 2,6-Dimethylbenzyl alcohol (2.76 g, 20.3 mmol) and diisopropyl azodicarboxylate (DIAD, 4.7 g, 23.2 mmol) in THF (20 ml) was added drop wise to a solution of 2-(3-hydroxyphenyl)-2-methylpropanenitrile (Step B, 3.2 g, 19.8 mmol) and triphenylphosphine (5.28 g, 20.1 mmol) in THF (50 ml) at 0° C. under argon. The reaction mixture was stirred at the same temperature for 16 hours, diluted with ether and washed with water. The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (hex:ethyl acetate, 9:1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115072B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-076f505952f641cca4d3f57da3eb9769 |
| Source note | uspto-grants-2015_08 |