HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetaldehyde → 3-Phenylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Phenylindole | HCID 96502 | 48% |
Reaction Steps
A solution of phenylhydrazine (1 mL, 10.15 mmol) and phenylacetaldehyde (1.32 mL, 10.15 mmol) in acetic acid was refluxed for 6 hours under a nitrogen atmosphere. After cooling to room temperature, the reaction mixture was poured into a saturated aqueous solution of sodium carbonate (100 mL) at 0° C. After extraction with dichloromethane (2×30 mL), the organic layer was dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to afford the desired indole (1a) as a pale oil (940 mg, 4.86 mmol, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-7e43f1a3e5394584957a94950323f391 |
| Source note | uspto-grants-2016_01 |