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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402793Erstellt: 25. Oktober 2026

Potassium Carbonate → 8-Cyclopropyl-2,2-dimethylchroman-6-carbaldehyde

https://huagongshe.com/reaction/402793

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
EduktPotassium cyclopropyltrifluoroborateHCID 23697338—
Edukt8-Chloro-2,2-dimethylchroman-6-carbaldehydeHCID 77230856—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelCyclopropyl methyl etherHCID 68323—
Produkt8-Cyclopropyl-2,2-dimethylchroman-6-carbaldehydeHCID 77230855—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A vial was charged with Pd(OAc)2 (7.99 mg, 0.04 mmol), XPhos (25.5 mg, 0.05 mmol), potassium carbonate (148 mg, 1.07 mmol), potassium cyclopropyltrifluoroborate (58.0 mg, 0.39 mmol) and 8-chloro-2,2-dimethyl-3,4-dihydro-2H-chromene-6-carbaldehyde (80 mg, 0.36 mmol). The mixture was dissolved in cyclopropylmethyl ether (1.62 mL) and water (0.16 mL) and purged with Ar. The reaction mixture was then stirred at 100° C. overnight, cooled to room temperature and filtered through a pad of celite. The filtrate was concentrated under vacuum, and the crude residue was purified by silica gel chromatography eluting with 0-20% EtOAc/hexanes to afford the desired product as a pale-yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08742110B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-1d789b5d164446f4ab2bade875d161c1
Quellennotizuspto-grants-2014_06