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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273367Erstellt: 25. Oktober 2026

3,4-dihydro-2H-pyran → 2-(4-bromo-3-methylphenoxy)tetrahydro-2H-pyran

https://huagongshe.com/reaction/273367

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-dihydro-2H-pyranHCID 8080—
Edukt4-Bromo-m-cresolHCID 72857—
KatalysatorBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(4-bromo-3-methylphenoxy)tetrahydro-2H-pyranHCID 23111838104,1%

Reaktionsschritte

A solution of 4-bromo-3-methylphenol (4.72 g, 25.2 mmol), 3,4-dihydro-2H-pyran (3.18 g, 37.8 mmol) and pyridinium p-toluenesulfonate (0.628 g, 2.50 mmol) in dichloromethane (100 mL) was stirred at room temperature for 24 hrs. The reaction mixture was washed with water, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (7.11 g, including unreacted 3,4-dihydro-2H-pyran) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456218B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-0b72634dd7964a618505719e779f1f36
Quellennotizuspto-grants-2008_11