Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 252256Erstellt: 23. Oktober 2026

Diethyl Ether → 958651-12-2

https://huagongshe.com/de/reaction/252256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktSulfuryl chlorideHCID 24648—
Edukt1-Bromo-3-cyclopropylbenzeneHCID 3282672—
EduktButyllithiumHCID 178418339—
LösungsmittelHexaneHCID 8058—
LösungsmittelEther tetrahydrofuranHCID 21868444—
Produkt958651-12-2HCID 55279574—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Bromo-3-cyclopropyl-benzene (1.0 g, 5.1 mmol) [prep.: J. Org. Chem. vol. 41, 2262-6 (1976)] was dissolved in dry THF/diethyl ether (1:1, 30 ml) under an argon atmosphere and cooled to −78° C. BuLi (1.6 M in hexanes, 3.2 ml, 5.1 mmol) was added dropwise and the reaction mixture was further stirred at low temperature for 15 min. This reaction mixture was added via cannula to a SO2 gas saturated solution of diethyl ether (20 ml) precooled to −78° C. The reaction mixture was stirred overnight at room temperature and concentrated under reduced pressure. The crude intermediate was suspended in n-hexane (4A sieves dried, 20 ml) and chilled (ice-water). A solution of sulfuryl chloride (0.3 ml, 3.6 mmol) in dry hexane (8 ml) was added dropwise to the stirred suspension and then the cold bath was removed. After 90 min at room temperature the reaction mixture was filtered (Speedex pad) and the filtrate was concentrated under reduced pressure to yield a yellow oil: 0.6 g, (67%) GC-MS: M=216.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07868030B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-94a9bcc3299841feb1fdc0123fafc4a7
Quellennotizuspto-grants-2011_01