HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 1h-Indole-3-acetic acid,2-phenyl-,ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Ethyl (2-bromo-1H-indol-3-yl)acetate | HCID 53994886 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1h-Indole-3-acetic acid,2-phenyl-,ethyl ester | HCID 12502669 | 81% |
Reaction Steps
To a solution of 2.0 g (7.1 mmol) of ethyl (2-bromoindol-3-yl)acetate in 40 ml of dioxane was added under argon 1.2 g (0.11 mmol) of Pd(PPh3)4 and 13.3 ml of 2.0 M sodium carbonate. After stirring at room temperature for ca. 15 min, 1.3 g (11 mmol) of benzeneboronic acid was added, and the mixture was heated at 80° C. under argon overnight. The mixture was cooled to room temperature and solids were removed by filtration. The filtrate was concentrated and chromatographed on silica gel with toluene as an eluent to yield 1.6 g (81%) of the 2-phenyl indole as a yellow crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410562B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-fd2b2434d51e4ab8bdf44da49d132eb7 |
| Source note | uspto-grants-2002_06 |