HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 4-(5-(Ethoxycarbonyl)-1H-pyrrol-3-yl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 5-(Ethoxycarbonyl)-gamma-oxo-1H-pyrrole-3-butanoic acid | HCID 23908396 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(5-(Ethoxycarbonyl)-1H-pyrrol-3-yl)butanoic acid | HCID 15272822 | 30.3% |
Reaction Steps
Into a 2000-mL 4-necked round-bottom flask was placed a solution of 113g (105 g, 438.92 mmol, 1.00 equiv) in CF3COOH (1000 mL), followed by the addition of triethylsilane (204 g, 1.75 mol, 4.00 equiv) dropwise with stirring at room temperature over 30 min (FIG. 14). The resulting solution was stirred at room temperature for 8 h, concentrated under vacuum and diluted with 500 mL of water and 500 mL of ethyl acetate. The pH value of the solution was adjusted to 7 with saturated aqueous sodium bicarbonate. The resulting solution was extracted with 3×500 mL of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum to afford 30 g (30%) of 113h as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729072B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-7a955e6ec04445988790a06989191479 |
| Source note | uspto-grants-2014_05 |