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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3001Erstellt: 23. Oktober 2026

Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde

https://huagongshe.com/de/reaction/3001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDihydrobenzofuranHCID 10329—
EduktMethane, dichloromethoxy-HCID 21004—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,3-Dihydrobenzofuran-5-carboxaldehydeHCID 73590160,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of α,α-dichloromethyl methyl ether (2.15 g, 19 mmol, 1.35 eq) in methylene chloride (30 mL) at -40° C. was added successively stannic chloride (1.65 g, 17 mmol, 1.2 eq) and 15 minutes later, a solution of 2,3-dihydrobenzofuran (1.68 g, 14 mmol) in CH2Cl2 (5 mL) maintaining the temperature at or below -35° C. The mixture was warmed to 0° C., stirred 1 hour, then poured into ice-water, and stirred a further 30 minutes. The mixture was diluted with ether, and the phases separated. The organic phase was concentrated in vacuo, and the residue purified by vacuum distillation to yield the title compound (1.25 g, 60%) as a colorless liquid. b.p. 119°-121° C. at 0.3 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731434
Quelldatensatzuspto-grants-1998_03
ORD IDord-a77e34e2ec91434fa697b43c33d45133
Quellennotizuspto-grants-1998_03