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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1405404Erstellt: 24. Oktober 2026

Isobutyraldehyde trimethylsilyl enol ether → Benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate

https://huagongshe.com/de/reaction/1405404

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutyraldehyde trimethylsilyl enol etherHCID 99685—
EduktBenzyl 4-bromo-3-methoxybenzoateHCID 58551480—
KatalysatorZinc(II) fluorideHCID 10129912—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoateHCID 86668528—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a flask purged with nitrogen was added Pd(tBu3P)2 (26 mg, 0.050 mmol), ZnF2 (52 mg, 0.50 mmol) and DMF (4 mL). The reaction mixture was allowed to stir for 10 minutes before benzyl 4-bromo-3-methoxy-benzoate (323 mg, 1.01 mmol) was added followed by trimethyl(2-methylprop-1-enoxy)silane (277 μL, 1.51 mmol). The reaction was heated at 80° C. overnight. The crude mixture was quenched with brine and extracted with EtOAc 3 times. The organic layer was dried over sodium sulfate and the solvent was evaporated to give benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate. ESI-MS m/z calc. 312.4, found 313.4 (M+1)+; Retention time: 3.27 minutes (4 min run).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08916565B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-a69e54d1aad34fee997f6f535585fb9b
Quellennotizuspto-grants-2014_12