HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488230Generated: October 30, 2026
3-Furancarboxaldehyde, 5-(triethylsilyl)- → HCID 11830655, compound
https://huagongshe.com/reaction/488230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Furancarboxaldehyde, 5-(triethylsilyl)- | HCID 10878438 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 11830655 | HCID 11830655 | — |
Reaction Steps
n-Butyl lithium (a 2.5 M solution in hexane; 4.4 ml, 11.0 mmol) was added dropwise to a suspension of methyltriphenylphosphonium bromide (3.93 g, 11 mmol) in THF (40ml) at 0 degrees C. under argon. After 2 hours stirring at 0 degrees C., a solution of 2-triethylsilyl-4-furaldehyde (1.54 g, 7.33 mmol) in THF (2 ml) was added. Stirring was continued at room temperature for 14 hours and the mixture was quenched with methanol/water 40 ml (1:1). Extraction (pentane) and evaporation of the dried (magnesium sulfate) extracts gave a residue, which was purified by flash chromatography on silica using pentane to give the titled furan. Rf (pentane) 0.75.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298633 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-ea9c3d33aa89439487fe9813971e5d96 |
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| Source note | uspto-grants-1994_03 |
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