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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490992Erstellt: 23. Oktober 2026

N-Methoxy-N-methylacetamide → 1-(2,2-Dimethyl-2,4-dihydro-1,3-benzodioxin-6-yl)ethan-1-one

https://huagongshe.com/de/reaction/490992

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Methoxy-N-methylacetamideHCID 537505—
Edukt6-Bromo-2,2-dimethyl-4H-benzo[d][1,3]dioxineHCID 14520338—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(2,2-Dimethyl-2,4-dihydro-1,3-benzodioxin-6-yl)ethan-1-oneHCID 21880610—

Reaktionsschritte

To the product of step (a) (110 g, 0.46 mol) in 1.0 L of THF at −78° C. was added 236 mL (0.51 mol) of 2.14 M n-butyllithium in hexanes via a dropping funnel. After 30 minutes, N-methyl-N-methoxy acetamide (71 g, 0.69 mol, available from TCI) was added. After 2 hours, the reaction mixture was quenched with water, diluted with 2.0 L of 1.0 M aqueous phosphate buffer (pH=7.0) and extracted once with diethyl ether. The diethyl ether phase was washed once with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give a light orange oil. The oil was dissolved in a minimum volume of ethyl acetate, diluted with hexanes, and to give the title compound as a crystalline solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07528253B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-4a2edf8a96af45adb0600e1fa74cbeb1
Quellennotizuspto-grants-2009_05