HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031499Generated: October 26, 2026
2-Chlorophenol → 2-(2-Chlorophenoxy)-5-(3,4-dimethoxybenzoyl)pyridine
https://huagongshe.com/reaction/1031499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorophenol | HCID 7245 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-5-(3,4-dimethoxybenzoyl)pyridine | HCID 14823221 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Chlorophenoxy)-5-(3,4-dimethoxybenzoyl)pyridine | HCID 14878846 | 82.6% |
Reaction Steps
In dimethyl formamide (10 ml) was suspended 60% sodium hydride (dispersion in paraffin) (288 mg), to which was added dropwise a solution of 2-chlorophenol (926 mg) in dimethylformamide. When exothermic reaction and evolution of hydrogen gas ceased, 2-chloro-5-(3,4-dimethoxybenzoyl)pyridine (1 g) was added to the reaction mixture, followed by stirring for hours at 80° C. The reaction mixture was poured into ice-water, then precipitating substance was collected by filtration, and purified by means of a silica gel column chromatography [eluent: n-hexane+ethyl acetate (1:1)] to obtain 2-(2-chlorophenoxy)-5-(3,4-dimethoxybenzoyl)pyridine (1.1 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04954497 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-79cd20f6fb6541acadbc883eb00f7b3f |
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| Source note | uspto-grants-1990_09 |
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