HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → 5-(Trimethylsilyl)furan-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 5-Bromofuran-3-carbaldehyde | HCID 15037056 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
Reaction Steps
To a stirred solution of 5-bromo-3-furaldehyde, dimethyl acetal (1.26 g., 5.7 mmol) in 10 ml dry tetrahydrofuran at 78° under argon was added t-butyllithium (9.69 mmol in pentane), followed by the subsequent addition of trimethylsilyl chloride (1.36 g., 12.54 mmol). After two hours the reaction was quenched with a 10% ammonium chloride solution and the organic portion was washed with 5% sodium bicarbonate, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give a yellow oil. Purification by flash chromatography (10% ether/pet. ether) yielded the desired aldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134128 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-f09d0f6dd0cf41afaf26091bc5580437 |
| Source note | uspto-grants-1992_07 |