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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835412Generated: November 4, 2026

Water → 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-methylthio-4-trifluoromethylpyridine

https://huagongshe.com/reaction/1835412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantSodium methanethiolateHCID 4378561—
Reactant3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-chloro-4-trifluoromethylpyridineHCID 12151533—
SolventEthyl AcetateHCID 8857—
Product3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-methylthio-4-trifluoromethylpyridineHCID 1215154258.3%

Reaction Steps

Sodium methanethiolate (0.32 g) was added to a dimethylformamide (15 ml) solution of 0.9 g of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-2-chloro-4-trifluoromethylpyridine (compound No. 11) at room temperature, followed by stirring for 1 hour. The mixture was poured into water (50 ml), and extraction with ethyl acetate was carried out. The ethyl acetate phase was dried over sodium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 0.54 g (yield 58%) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-2-methylthio-4-trifluoromethylpyridine (compound No. 50; pale yellow oily substance), and its structure was confirmed by nuclear magnetic resonance spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770662B2
Source datasetuspto-grants-2004_08
ORD IDord-cdee8d535ef3414f8a70a9c534dbc349
Source noteuspto-grants-2004_08