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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716561Generated: October 30, 2026

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

https://huagongshe.com/reaction/716561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
Reactant(6-Bromopyridin-2-yl)methanolHCID 3517811—
SolventDichloromethaneHCID 6344—
Product2-Bromo-6-((methoxymethyloxy)methyl)pyridineHCID 8667111798.4%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187690B2
Source datasetuspto-grants-2015_11
ORD IDord-06a7affd5aaf444bac573d4d2315c20d
Source noteuspto-grants-2015_11