HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → Ethyl 5-bromo-2-ethylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Ethyl 5-bromo-2-(1-hydroxyethyl)thiophene-3-carboxylate | HCID 68509503 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Ethyl 5-bromo-2-ethylthiophene-3-carboxylate | HCID 68515411 | 94% |
Reaction Steps
To a solution of ethyl 5-bromo-2-(1-hydroxyethyl)thiophene-3-carboxylate (11.0 g) synthesized above in trifluoroacetic acid (100 mL) was added dropwise triethylsilane (18.8 mL). After stirring at room temperature for 1 hr, the reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:19, volume ratio) to give the title compound (9.67 g, 94%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309580B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-481dde5857e24b4090753329b6f77817 |
| Source note | uspto-grants-2012_11 |