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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561927Erstellt: 26. Oktober 2026

Ethyl orthoformate → 3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenol

https://huagongshe.com/reaction/561927

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl orthoformateHCID 31214—
EduktNeopentyl glycolHCID 31344—
Edukt6-Bromo-2-hydroxy-3-methoxybenzaldehydeHCID 262237—
Katalysatorp-Toluenesulfonic acidHCID 6101—
Produkt3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenolHCID 59761836100%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 6-bromo-2-hydroxy-3-methoxy-benzaldehyde (2.31 g, 10.0 mmol), neopentyl glycol (1.14 g, 11.0 mmol), TsOH (9.5 mg) and triethyl orthoformate (1.93 g, 13.0 mmol) were heated at 110° C. for 30 min and then partitioned between NaHCO3 (300 mL) solution and EtOAc (200 mL). The aqueous layer was extracted with EtOAc (3×30 mL) and the combined extracts were washed with brine and dried through Na2SO4. Evaporation of solvent afforded the title compound (3.17 g, 100%). 1H NMR (CDCl3) δ 0.85 (s, 3H), 1.27 (s, 3H), 3.70 (s, 2H), 3.82 (s, 2H), 3.85 (s, 3H), 5.90 (s, 1H), 6.72 (d, J=8 Hz, 1H), 7.02 (d, J=8 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063225B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-8ce3b895fef84432bf23310f1f69fcac
Quellennotizuspto-grants-2011_11