HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(5-Bromo-4-chloro-2-methoxymethoxybenzoyl)-3-methoxymethoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(5-Bromo-4-chloro-alpha-cyano-2-methoxymethoxybenzyl)-3-methoxymethoxypyridine | HCID 10670177 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5-Bromo-4-chloro-2-methoxymethoxybenzoyl)-3-methoxymethoxypyridine | HCID 10835743 | — |
Reaction Steps
DMF (100 ml) was added to a mixture of 2-(5-bromo-4-chloro-α-cyano-2-methoxymethoxybenzyl)-3-methoxymethoxypyridine (10.1 g) and potassium carbonate (9.84 g). The mixture was stirred at room temperature overnight under oxygen atmosphere. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous saline solution, dried (anhydrous magnesium sulfate), and concentrated. The concentrate was purified by a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 2-(5-bromo-4-chloro-2-methoxymethoxybenzoyl)-3-methoxymethoxypyridine (9.08 g, m.p. 70°-72° C.). The spectrum data are shown as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716971 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-6bf6bd41ec3b4f6d8dc0724dfd18e59b |
| Source note | uspto-grants-1998_02 |