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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2408248Erstellt: 25. Oktober 2026

Phosphoric Acid → 1-[1-(Allyloxy)-2-methyl-2-propenyl]-4-methylbenzene

https://huagongshe.com/reaction/2408248

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphoric AcidHCID 1004—
EduktAllyl chlorideHCID 7850—
Edukt2-Methyl-1-(4-methylphenyl)prop-2-en-1-olHCID 54023324—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt1-[1-(Allyloxy)-2-methyl-2-propenyl]-4-methylbenzeneHCID 6733042180,2%

Reaktionsschritte

Solid sodium tert-butylate (66.65 g, 0.589 mol) was dissolved under nitrogen in dry THF (350 ml) and 1-(4-methylphenyl)-2-methyl-2-propen-1-ol (41.16 g, 0.239 mol) in dry THF (25 ml) was added in 15 minutes without external cooling. The reaction was further stirred at room temperature for 50 minutes. Tetra butyl ammonium iodide (5.04 g, 0.014 mol) was added followed by allyl chloride (40 g, 0.518 mol) in 25 minutes (exothermic to 47° C.). The reaction was stirred for 24 hours, before adding more tetra butyl ammonium iodide (2.30 g, 0.006 mol) and allyl chloride (9.30 g, 0.120 mol). After stirring for 24 hours at room temperature, the reaction was poured onto ice, diluted with MTBE and acidified with aqueous phosphoric acid. The organic phase was washed with brine, saturated aqueous sodium bicarbonate and brine and dried over solid anhydrous sodium sulfate. The solid was filtered off, rinsed with MTBE and solvents were removed under vacuum. The product was purified by distillation through a 35-cm Fisher column. 38.78 g of the desired allyl ether were obtained (yield=80%). B.P.=79° C./1.6 mbar

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08815792B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-563d9c62427f4feea5896d68521d16c0
Quellennotizuspto-grants-2014_08