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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 334694Erstellt: 25. Oktober 2026

Iodine → 1-Quinoxalin-2-yl-but-3-yn-1-ol

https://huagongshe.com/reaction/334694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktPropargyl bromideHCID 7842—
EduktAmmonium ChlorideHCID 25517—
EduktQuinoxaline-2-carbaldehydeHCID 594088—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Quinoxalin-2-yl-but-3-yn-1-olHCID 8663024714,2%

Reaktionsschritte

To a mixture of magnesium (229 mg, 9.41 mmol), mercuric chloride (13 mg, 47 μmol) and few crystals of iodine in Et2O (1.5 mL), a solution of propargyl bromide (0.53 mL, 5.88 mmol) in Et2O (4.5 mL) was added slowly in order to maintain a reflux. The reaction mixture was stirred 1 hour and added to a solution of quinoxaline-2-carbaldehyde (500 mg, 3.16 mmol) in THF (2 mL). The resulting reaction mixture was stirred at 0° C. for 30 min., at room temperature for 30 min. and was poured onto saturated NH4Cl solution. The aqueous phase was extracted with Et2O. The aqueous phase was washed with water, brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by C18 flash chromatography (H2O/acetonitrile 100:0 to 80:20) to yield 90 mg (0.45 mmol, 14%) of 1-quinoxalin-2-yl-but-3-yn-1-ol as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883826B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-0f3a9936008745609b7dd2a151345d65
Quellennotizuspto-grants-2014_11