HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylphosphine → 5-Allyloxy-1-[(2-thiophen-3-yl)ethyl]-1h-indole-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Thiophene-3-ethanol | HCID 83731 | — |
| Reactant | Ethyl 5-[(prop-2-en-1-yl)oxy]-1H-indole-2-carboxylate | HCID 13286893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Allyloxy-1-[(2-thiophen-3-yl)ethyl]-1h-indole-2-carboxylic acid ethyl ester | HCID 12094465 | 94% |
Reaction Steps
To solution of 5-allyloxyindole-2-carboxylic acid ethyl ester (1.0 g, 4.08 mmol) in THF (10 mL) was added azodicarboxylic acid bis[dimethylamide] (TMAD; 1.4 g, 8.15 mmol). After stirring at room temperature for 20 min, 2-(3-thienyl)ethanol (0.78 g, 6.12 mmol) was added followed by the addition of tributyl phosphine (1.65 g, 8.15 mmol). After stirring at room temperature for 18 h, the reaction was partitioned between ethyl acetate and water. The organic layer was washed with brine and dried over Na2SO4. Purification by flash colunmn chromatography (silica gel, EtOAc/hexanes) yielded the desired product as an oil (1.36 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06670388B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-2659ad643eac46948a902f9d8b56e9fb |
| Source note | uspto-grants-2003_12 |