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HRID 241401作成日:2026年10月26日

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

https://huagongshe.com/reaction/241401

反応式

関与物質

役割名称HCID仕込み量
反応物Chloromethyl Methyl EtherHCID 7864—
反応物DiisopropylethylamineHCID 81531—
反応物(6-Bromopyridin-2-yl)methanolHCID 3517811—
溶媒DichloromethaneHCID 6344—
生成物2-Bromo-6-((methoxymethyloxy)methyl)pyridineHCID 8667111798.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648194B2
出典データセットuspto-grants-2014_02
ORD IDord-f5b4bcab9f3940baa11e653db57a3168
出典メモuspto-grants-2014_02