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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241401Erstellt: 25. Oktober 2026

Chloromethyl Methyl Ether → 2-Bromo-6-((methoxymethyloxy)methyl)pyridine

https://huagongshe.com/reaction/241401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloromethyl Methyl EtherHCID 7864—
EduktDiisopropylethylamineHCID 81531—
Edukt(6-Bromopyridin-2-yl)methanolHCID 3517811—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Bromo-6-((methoxymethyloxy)methyl)pyridineHCID 8667111798,4%

Reaktionsschritte

Under a stream of argon, (6-bromopyridine-2-yl)methanol (10 g; 53.2 mmol) was dissolved in methylene chloride (50 mL). Diisopropylethylamine (9.6 g; 74.5 mmol) and chloromethyl methyl ether (5.35 g; 66.5 mmol) were added to the reaction mixture in an ice bath, and further, the reaction mixture was stirred at room temperature for 17 hours. The reaction solution was poured into ice water and extracted with chloroform. The organic layer was washed with water, dried over sodium sulfate, and then evaporated under reduced pressure. The resulting residue was separated and purified by silica gel column chromatography (SiO2, 200 g) (toluene/ethyl acetate=10/1) to give 12.15 g (yield: 98%) of the title compound (11).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08648194B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-f5b4bcab9f3940baa11e653db57a3168
Quellennotizuspto-grants-2014_02