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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250521Erstellt: 24. Oktober 2026

Methanol → 2-Methyl-2-(4-methylphenyl)-1,3-dioxane

https://huagongshe.com/de/reaction/250521

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Eduktp-METHYLACETOPHENONEHCID 8500—
Edukt1,3-PropanediolHCID 10442—
EduktN-bromobutanimideHCID 67184—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Methyl-2-(4-methylphenyl)-1,3-dioxaneHCID 34665425%

Reaktionsschritte

To a stirred mixture of 4-methylacetophenone (1.3 mL, 10 mmol), triethylformate (2.0 mL, 12 mmol), 1,3-propanediol (2.2 mL, 30 mmol) and dry methanol (1.2 mL) in dry dichloromethane (50 mL) was added NBS (53 mg, 0.30 mmol). The mixture was protected from light and stirred at room temperature under an inert atmosphere of nitrogen for 70 h. After the mixture was washed with saturated sodium bicarbonate solution (20 mL), the aqueous phase was extracted with dichloromethane (3×30 mL). The combined organic solution was washed with water (2×20 mL), brine (1×20 mL), then dried (Na2SO4) and concentrated under reduced pressure. Flash column chromatography of the residue, eluting with 37% aqueous ammonia:ether:hexane (0.02:1:6) afforded 2-methyl-2-(4-methylphenyl)-1,3-dioxane (22) as a colourless oil (480 mg, 24%). 1H nmr (200 MHz, CDCl3) 1.50 (s, 3H, CH3), 1.96-2.25 (m, 2H, OCH2CH2CH2O), 2.37 (s, 3H, ArCH3), 3.70-4.00 (m, 4H, OCH2CH2CH2O), 7.23 (d, J=8.3 Hz, 2H, 2×ArH), 7.33 (d, J=8.3 Hz, 2H, 2×ArH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863313B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-ffaa6a0b286f4c22bdd015edf5bdc355
Quellennotizuspto-grants-2011_01