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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-chloro-4-trifluoromethylpyridine | HCID 12151533 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-methylthio-4-trifluoromethylpyridine | HCID 12151542 | 58.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770662B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-cdee8d535ef3414f8a70a9c534dbc349 |
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| Source note | uspto-grants-2004_08 |
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