HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 348248Erstellt: 24. Oktober 2026
Iodine → (5R)-2-iodo-6-methyl-7-(2-methylthiazol-4-yl)-5-(triethylsilyloxy)-2,6-heptadiene
https://huagongshe.com/de/reaction/348248
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Edukt | (3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enal | HCID 86586609 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Ethyltriphenylphosphonium iodide | HCID 78474 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (5R)-2-iodo-6-methyl-7-(2-methylthiazol-4-yl)-5-(triethylsilyloxy)-2,6-heptadiene | HCID 86586611 | — |
Reaktionsschritte
To a suspension of ethyltriphenylphosphonium iodide (7.90 g) in THF (150 mL) is added n-butyllithium (7.17 mL, 2.5 M in hexane) at ambient temperature. After disappearance of the solid material, the red solution is cannulated into a vigorously stirred solution of iodine (4.54 g) in THF (150 mL) at −78° C. The resulting dark brown suspension is stirred for 5 minutes and allowed to warm gradually to −30° C. A solution of sodium hexamethyldisilazide (17.3 mL, 1.0 M in THF) is added dropwise to afford a dark red solution. A solution of (3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enal (2.0 g) in THF (10 mL) is slowly added, and stirring is continued at −30° C. for 30 minutes. The reaction mixture is diluted with pentane (100 mL), filtered through a pad of Celite, and concentrated. Purification by flash column chromatography on SiO2 (hexane/ethyl acetate, 15:1) affords the vinyl iodide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07176235B2 |
|---|
| Quelldatensatz | uspto-grants-2007_02 |
|---|
| ORD ID | ord-a5069b305f724da99decc21ed307992b |
|---|
| Quellennotiz | uspto-grants-2007_02 |
|---|