HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243784Generated: October 29, 2026
Toluene → 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine
https://huagongshe.com/reaction/243784
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Hexamethylphosphorous triamide | HCID 15355 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-3-chloro-5-trifluoromethylpyridine | HCID 12151303 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine | HCID 12151304 | 64% |
Reaction Steps
16.4 g (304 mmol) of sodium methoxide was added to a toluene 150 ml solution of 18.5 g (47.5 mmol) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-chloro-5-trifluoromethylpyridine obtained in Step (c) and 16.6 ml (95.4 mmol) of hexamethylphosphorous triamide, followed by stirring under reflux with heating for 30 minutes. Water was added to terminate the reaction, and the aqueous layer was extracted with ethyl acetate. Then, the organic layer was dried over anhydrous sodium sulfate and subjected to filtration, and the solvent was distilled off under reduced pressure. The crude product was purified by silica gel column chromatography to obtain 11.7 g (yield: 64%) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine (melting point: 103 to 106° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653277B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-11044d52482149d4a5f3b93cddb9cc3e |
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| Source note | uspto-grants-2014_02 |
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