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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357233Erstellt: 23. Oktober 2026

Chlorotrimethylsilane → 2-Trimethylsilyloxy-4-(4-(methylthio)phenyl)-3,4-dihydrofuran

https://huagongshe.com/de/reaction/357233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktPentaneHCID 8003—
Edukt2(5H)-FuranoneHCID 10341—
Edukt4-BromothioanisoleHCID 66037—
EduktSodium BicarbonateHCID 516892—
EduktHCID 178418306HCID 178418306—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTriethylamineHCID 8471—
Produkt2-Trimethylsilyloxy-4-(4-(methylthio)phenyl)-3,4-dihydrofuranHCID 18400192—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 3.86 g (19 mmol) of 4-bromothioanisole in 90 mL of Et2O cooled at -78° C., is added 22 mL of 1.7M solution of t-BuLi in pentane (38 mmol) dropwise. The reaction mixture is stirred for 15 min at -78° C. and 3.8 g of CuI is added and the reaction mixture is allowed to warm to -40° C. over a period of 30 min. A solution of 1.7 g of 2(5H)-furanone in 10 ml of THF is added. After stirring for 1 h, 2 ml of freshly distilled TMSCl is added dropwise. The reaction mixture is then treated with 2 ml of Et3N and 50 ml of sat. NaHCO3, and extracted with 100 ml of ether. The ether layer is dried over Na2SO4 and concentrated to the crude title compound which is used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840746
Quelldatensatzuspto-grants-1998_11
ORD IDord-0b462194545542c6a12333c590a0d785
Quellennotizuspto-grants-1998_11