HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3-(3-(2,6-Dimethylbenzyloxy)phenyl)propanenitrile
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 | 3-(3-Hydroxyphenyl)propanenitrile | HCID 1712312 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3-(2,6-Dimethylbenzyloxy)phenyl)propanenitrile | HCID 66959389 | — |
Reaction Steps
A solution of 3-(3-hydroxyphenyl)propanenitrile (Step B, 1.25 g, 8.5 mmol) and diisopropyl azodicarboxylate (DIAD, 1.87 g, 9.26 mmol) in dry THF (10 ml) was added drop wise to a solution of 2,6-Dimethylbenzyl alcohol (1.27 g, 9.3 mmol) and triphenylphosphine (TPP, 2.43 g, 9.26 mmol) in dry THF (30 ml) at 0° C. under argon. The reaction mixture was warmed to room temperature for 4 hours or until all the starting material is consumed, diluted with ether and washed with water (2×). The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (hex: ethyl acetate 2:1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889724B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-56fc9acd305a4bdb9d2318da9900a240 |
| Source note | uspto-grants-2014_11 |