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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835427Generated: November 4, 2026

Dimethylformamide → 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2,3-dichloro-5-methoxypyridine

https://huagongshe.com/reaction/1835427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-chloro-5-methoxypyridine-N-oxideHCID 23503588—
SolventTolueneHCID 1140—
Product4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2,3-dichloro-5-methoxypyridineHCID 23503595739.8%

Reaction Steps

5 ml of dimethylformamide was added to 2.5 ml of toluene, the mixture was cooled with ice, and 1.3 ml (1.4 mmol) of phosphorus oxychloride was dropwise added thereto. After the mixture was stirred under cooling with ice for 10 minutes, 2.5 g (0.7 mmol) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-chloro-5-methoxypyridine-N-oxide was added thereto. After the mixture was stirred under cooling with ice for 30 minutes, the temperature was recovered to room temperature, followed by stirring for 2 hours. 30 ml of water was added to the mixture to terminate the reaction, and ethyl acetate was added thereto for extraction. The organic layer was dried over anhydrous sodium sulfate, subjected to filtration and purified by silica gel column chromatography to obtain 2.0 g (yield 76%) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-2,3-dichloro-5-methoxypyridine (compound No. 193; m.p. 98-99° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770662B2
Source datasetuspto-grants-2004_08
ORD IDord-4e29c744629d4a6ba339a90cd7aeb21d
Source noteuspto-grants-2004_08