HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835425Generated: November 2, 2026
Toluene → 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-3-chloro-5-methoxypyridine
https://huagongshe.com/reaction/1835425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 23503602 | HCID 23503602 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-3-chloro-5-methoxypyridine | HCID 23503593 | 690.4% |
Reaction Steps
5.0 g (2.8 mmol) of hexamethylphosphoric triamide and 1.1 g (2.1 mmol) of sodium methoxide were added to a toluene (60 ml) solution of 5.0 g (1.4 mmol) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3,5-dichloropyridine (compound No. 191), followed by stirring under reflux by heating for 5 hours. After the mixture was cooled, 50 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 and subjected to filtration, and the solvent was distilled off under reduced pressure. The crude product thus obtained was purified by silica gel column chromatography to obtain 3.4 g (yield 69%) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-chloro-5-methoxypyridine (compound No. 244; pale yellow oily substance).
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-4e419e4e46494ffa9f282ac9769be4de |
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| Source note | uspto-grants-2004_08 |
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