HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2216370Erstellt: 25. Oktober 2026
Benzyl Bromide → 2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine
https://huagongshe.com/reaction/2216370
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | 2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine | HCID 21942269 | — |
| Edukt | HCID 178419663 | HCID 178419663 | — |
| Katalysator | Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chloride | HCID 21654969 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine | HCID 21942262 | — |
Reaktionsschritte
A mixture of 6.3 g of 2-bromo-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine, 240 mg of 1,3-bis(diphenylphosphino)propanenickel (II) chloride and 20 ml of tetrahydrofuran was stirred in advance under nitrogen atmosphere in an ice bath. To this was added dropwise a diethyl ether solution of benzyl magnesium bromide prepared from 3.4 ml of benzyl bromide, 0.8 g of magnesium and 15 ml of diethyl ether, followed by stirring as it was at room temperature for overnight. The reaction mixture was partitioned between a saturated aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography with 5–10% ethyl acetate/hexane, to give 6.6 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07112593B2 |
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| Quelldatensatz | uspto-grants-2006_09 |
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| ORD ID | ord-7efc740474614fa8bb53d2db1bac1da8 |
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| Quellennotiz | uspto-grants-2006_09 |
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