HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloromethyl Methyl Ether → 2-Bromo-6-((methoxymethyloxy)methyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (6-Bromopyridin-2-yl)methanol | HCID 3517811 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-6-((methoxymethyloxy)methyl)pyridine | HCID 86671117 | 98.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187690B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-06a7affd5aaf444bac573d4d2315c20d |
| Source note | uspto-grants-2015_11 |