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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862074Generated: October 30, 2026

Dimethylformamide → 2-(5-Bromo-4-chloro-2-methoxymethoxybenzoyl)-3-methoxymethoxypyridine

https://huagongshe.com/reaction/862074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(5-Bromo-4-chloro-alpha-cyano-2-methoxymethoxybenzyl)-3-methoxymethoxypyridineHCID 10670177—
SolventWaterHCID 962—
Product2-(5-Bromo-4-chloro-2-methoxymethoxybenzoyl)-3-methoxymethoxypyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716971
Source datasetuspto-grants-1998_02
ORD IDord-6bf6bd41ec3b4f6d8dc0724dfd18e59b
Source noteuspto-grants-1998_02