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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 237861Erstellt: 26. Oktober 2026

Iodoethane → Methyl acetate hexane

https://huagongshe.com/reaction/237861

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktSodium hydrideHCID 24758—
Edukt4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-olHCID 11123315—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl acetate hexaneHCID 234493021%
Produkt2-(4-Ethoxy-but-2-ynyloxy)-tetrahydro-pyranHCID 68529463—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

An oven dried 500 ml RBF was charged with NaH (60% in mineral oil) (1.41 g, 35.3 mmol) and suspended in DMF (100 mL). The mixture was cooled to 0° C. and 4-(tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol (prepared in accordance with the procedures of Tamaru et al., Bull. Chem. Soc. Jpn., 1995, 1689-1705) (6.0 g, 35.3 mmol) was added. The reaction mixture was allowed to reach room temperature and stirred for one hour. To the mixture was added iodoethane (20.8 g, 133 mmol). The reaction mixture was stirred for 3.5 hours at room temperature before being quenched with ice/H2O and extracted with MeOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated. Silica gel chromatography (1-20% MeOAc/hexane) provided 4.71 g of 2-(4-ethoxy-but-2-ynyloxy)-tetrahydro-pyran as a clear oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642603B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-fd436759d4e74f2f98770a0ccab266a0
Quellennotizuspto-grants-2014_02