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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1843970Erstellt: 27. Oktober 2026

p-Toluenesulfonic acid → 3-Bromo-4-(dimethoxymethyl)pyridine

https://huagongshe.com/reaction/1843970

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktEthyl AcetateHCID 8857—
Edukt3-Bromopyridine-4-carboxaldehydeHCID 2762997—
LösungsmittelMethanolHCID 887—
LösungsmittelHexaneHCID 8058—
Produkt3-Bromo-4-(dimethoxymethyl)pyridineHCID 2071514596,3%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

p-Toluene sulphonic acid (PTSA) (613.5 mg, 3.225 mmol) was added to a stirred solution of 3-bromoisonicotinaldehyde (500 mg, 2.688 mmol) in methanol (20 mL) and the resulting reaction mixture was stirred for 3 hours at 75° C. The reaction was monitored by TLC (10% ethyl acetate in hexane). The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The crude residue was diluted with ice, basified using saturated NaHCO3 solution and extracted using ethyl acetate. The organic layer was washed with water, brine solution, dried over Na2SO4 and concentrated under reduced pressure. Purification by column chromatography on silica gel (10% ethyl acetate in hexane) afforded 600 mg of the product (96.3% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08946260B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-94b7ec8671794e2c90f43b79de571854
Quellennotizuspto-grants-2015_02