HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181754Generated: October 27, 2026
Iodine → (6S)-3-iodo-6-(6-quinolyl)-6-(triethylsilyloxy)-3-hexene
https://huagongshe.com/reaction/2181754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | Triphenyl(propyl)phosphonium iodide | HCID 10982905 | — |
| Reactant | (3S)-3-(triethylsilyloxy)-3-(6-quinolyl)propanal | HCID 86586607 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6S)-3-iodo-6-(6-quinolyl)-6-(triethylsilyloxy)-3-hexene | HCID 86587399 | — |
Reaction Steps
A suspension of propyltriphenylphosphonium iodide (8.2 gm) in 150 mL of tetrahydrofuran is treated with a 2.5 M solution of n-butyllithium (7.17 mL) at ambient temperature. The resulting red solution is transferred via cannula into a vigorously stirred solution of iodine (4.54 gm) in 150 mL of tetrahydrofuran cooled to −78° C. The resulting suspension is stirred for 5 minutes, then gradually warmed to −30° C. A 1.0 M solution of sodium hexamethyldisilazide (17.3 mL) is then added dropwise to form a red solution. A solution of (3S)-3-(triethylsilyloxy)-3-(6-quinolyl)propanal (1.9 gm) in 10 mL of tetrahydrofuran is then added dropwise, and stirring is continued at −30° C. for 30 minutes. The mixture is diluted with ether, filtered through a pad of Celite, and concentrated. The product is purified by flash chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06893859B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-9a572146f6c349df8fa5ca8bbd67a359 |
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| Source note | uspto-grants-2005_05 |
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