HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Chloro-6-ethyl-3-methyl-2-(2,4,5-trimethyl-phenoxy)-pyridine 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,4,6-Trimethylphenol | HCID 10698 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Dichloro-6-ethyl-3-methyl-pyridine 1-oxide | HCID 21912305 | — |
| Product | 4-Chloro-6-ethyl-3-methyl-2-(2,4,5-trimethyl-phenoxy)-pyridine 1-oxide | HCID 22596025 | — |
Reaction Steps
To a solution of 2,4,6-trimethylphenol in dry THF was added NaH and stirred at room temperature for 20 minutes. A solution of 2,4-dichloro-6-ethyl-3-methyl-pyridine 1-oxide was added and the resulting mixture was heated at reflux for 1.5 hour. The mixture was cooled to room temperature, quenched with water, extracted with ethyl acetate. The organic layer was separated, dried and concentrated to give the title compound which was used directly for the next step reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06844351B1 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-12291451298a4acf8462b426fe4417c7 |
| Source note | uspto-grants-2005_01 |