HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-Octanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzenesulfonamide, N,4-dimethyl- | HCID 12543 | — |
| Reactant | 2-Octanol | HCID 20083 | — |
| Reactant | 2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamate | HCID 53384415 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Octanol | HCID 20083 | — |
| Product | N,4-dimethyl-N-octan-2-ylbenzenesulfonamide | HCID 11055596 | — |
Reaction Steps
After (racemic)-2-octanol (300 mg, 2.30 mmol), triphenylphosphine (727 mg, 2.76 mmol), N-methyl-p-toluenesulfonamide (514 mg, 2.76 mmol), and THF (12 ml) were added to a 50 ml flask, azodicarboxylic acid bis(2-methoxyethyl) ester (648 mg, 2.76 mmol) dissolved in THF (6 ml) was added dropwise thereto at 20° C., and the reaction was allowed to proceed for 21 hours. Subsequently, a crude product obtained by concentration was purified by column chromatography (silica gel, 10% ethyl acetate-hexane solution) to give 4,N-dimethyl-N-(1-methylheptyl)benzenesulfonamide as a white solid substance (223 mg, yield: 33%/(racemic)-2-octanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820802B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-0aa07f108c494dc6a76cdc33f2ad7e35 |
| Source note | uspto-grants-2010_10 |