HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylethanol → 3-Acetyl-5-chloro-1-phenethylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 1-(5-chloro-1H-indol-3-yl)ethanone | HCID 2762971 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Acetyl-5-chloro-1-phenethylindole | HCID 12968635 | 65% |
Reaction Steps
To a mixture of 0.58 g (3 mmol) of 3-acetyl-5-chloroindole, 1.42 g (5.4 mmol) of triphenylphosphine and 0.66 g (5.4 mmol) of phenethyl alcohol in THF (12 ml) was added under ice-cooling, 1.09 g (5.4 mmol) of diisopropyl azodicarboxylate. After stirring for 3 hours at room temperature, the mixture was concentrated under reduced pressure. The obtained residue was chromatographed on silica gel (1/4 ethyl acetate/toluene as eluant) to give 0.58 g of the titled compound as an oil. Yield: 65%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06333323B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-c0e267bbb3c347e38d37dac1d733be82 |
| Source note | uspto-grants-2001_12 |