HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084773Generated: October 30, 2026
Sodium Hydroxide → 6-Phenoxy-2-pyridylmethyl 2-ethyl-2-methylbutyl ether
https://huagongshe.com/reaction/1084773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,2-Diethyl-1-propanol | HCID 87605 | — |
| Reactant | 2-Chloromethyl-6-phenoxypyridine | HCID 13849241 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Phenoxy-2-pyridylmethyl 2-ethyl-2-methylbutyl ether | HCID 14879000 | 71.9% |
Reaction Steps
Under a nitrogen atmosphere, 3.83 g of a 45% aqueous sodium hydroxide solution, 120 mg of tetrabutylammonium bromide and 5 ml of toluene were mixed, and to the resulting mixture solution, a solution of 1.0 g of 2-ethyl-2-methylbutanol and 1.51 g of 6-phenoxy-2-chloromethylpyridine in 5 ml of toluene was added at room temperature. After stirring at room temperature for 16 hours, the reaction solution was poured into dilute hydrochloric acid-ice water and extracted twice with toluene. The toluene layers were combined, washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was subjected to column chromatography on silica gel (developing solvent, n-hexane: ethyl acetate=50:1) to obtain 1.48 g of desired 6-phenoxy-2-pyridylmethyl 2-ethyl-2-methylbutyl ether [present compound (35)] as a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05006538 |
|---|
| Source dataset | uspto-grants-1991_04 |
|---|
| ORD ID | ord-1b780f3b456c487b80e83376170b96df |
|---|
| Source note | uspto-grants-1991_04 |
|---|