HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dihydrobenzofuran | HCID 10329 | — |
| Edukt | Methane, dichloromethoxy- | HCID 21004 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,3-Dihydrobenzofuran-5-carboxaldehyde | HCID 735901 | 60,3% |
Reaktionsbedingungen
| Temperatur | 0 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05622971 |
| Quelldatensatz | uspto-grants-1997_04 |
| ORD ID | ord-aeae02a3858c4f9190646450ed5f9a61 |
| Quellennotiz | uspto-grants-1997_04 |