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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1393266Erstellt: 26. Oktober 2026

2-Bromo-cyclopent-2-enol → 2-Isobutyl-cyclopent-2-enol

https://huagongshe.com/reaction/1393266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-cyclopent-2-enolHCID 11137462—
EduktHCID 178418816HCID 178418816—
KatalysatorDichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Isobutyl-cyclopent-2-enolHCID 21986210—

Reaktionsschritte

The alcohol (Intermediate D3, 16 mmol) in THF (30 mL) at 0° C. was treated with isobutyl magnesium bromide (40 mmol). The catalyst, 1,3-bis(diphenylphosphino)propane nickel (II) chloride (0.75 mmol) (NiCl2dppp) was added in one portion and the mixture was heated to reflux for 3 h. (see: Organ et al. J. Org. Chem. 1997, 62, 1523, incorporated herein by reference). The reaction mixture was cooled to rt and quenched with sat. NH4Cl solution. The mixture was filtered and partitioned between brine and diethyl ether. The organic layer was removed and dried over Na2SO4, filtered and concentrated under vacuum. The oil was purified by chromatography on SiO2 with 20% EtOAc:Hx to yield 2-isobutyl-cyclopent-2-enol (Intermediate D4). Use of 2-isobutyl-cyclopent-2-enol (Intermediate D4) in Method A produced 4-(2-isobutyl-cyclopent-2-enylmethyl)-1,3-dihydro-imidazole-2-thione (Compound 20).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07345077B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-01f9c3eee9894caf88f9802cf277b36c
Quellennotizuspto-grants-2008_03