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Chloromethyl Methyl Ether → 2-Bromo-6-((methoxymethyloxy)methyl)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloromethyl Methyl Ether | HCID 7864 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (6-Bromopyridin-2-yl)methanol | HCID 3517811 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Bromo-6-((methoxymethyloxy)methyl)pyridine | HCID 86671117 | 98.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08648194B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-f5b4bcab9f3940baa11e653db57a3168 |
| 出典メモ | uspto-grants-2014_02 |