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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1829071Erstellt: 26. Oktober 2026

Acetaldehyde → 3-Methyl-1(3H)-isobenzofuranone

https://huagongshe.com/reaction/1829071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehydeHCID 177—
Edukt2-Bromobenzoic acidHCID 6940—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt3-Methyl-1(3H)-isobenzofuranoneHCID 1893935%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 2-bromobenzoic acid (0.50 g, 2.49 mmol) in THF (12.0 ml) cooled at −78° C. was added 2.5M n-BuLi in hexane (2.0 ml). After stirring for 25 minutes, a solution of acetaldehyde (0.142 g, 3.23 mmol) in THF (0.3 ml) was added. The reaction was allowed to warm to room temperature after 8 minutes at −78° C., and then quenched into 10% HCl aqueous solution (30 ml). The acidic solution was rapidly stirred for 1.5 hours, and then extracted with EtOAc. The combined organic layers were washed with saturated NaHCO3 aqueous solution, brine, dried with anhydrous Na2SO4, and rotary evaporated to an oily residue. Gradient chromatography of the oil residue through a silica gel column with 20% to 30% EtOAc in hexane afforded 3-methyl-2-benzofuran-1(3 H)-one as a clear oil (130 mg, 35%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07060844B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-afb47e42fae549839f4474ece4107bb4
Quellennotizuspto-grants-2006_06