HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → m-Phenoxybenzyl alpha-isopropyl-4-trifluoromethoxyphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-Phenoxybenzyl alcohol | HCID 26295 | — |
| Reactant | HCID 20343288 | HCID 20343288 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | m-Phenoxybenzyl alpha-isopropyl-4-trifluoromethoxyphenylacetate | HCID 20343285 | — |
Reaction Steps
To a solution of m-phenoxybenzyl alcohol (1.89 g) and pyridine (1 ml) in methylene chloride (6 ml) is added a methylene chloride (7 ml) solution of α-isopropyl-4-trifluoromethoxyphenylacetyl chloride, prepared from the corresponding acid (2.46 g) as illustrated in Example 15. After stirring the reaction mixture overnight, it is washed with water, diluted hydrochloric acid solution, dilute potassium hydroxide solution, water and evaporated to an orange oil. Purification by silica gel chromatography gives the desired ester (2.76 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04178460 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-22765441f38e4e9d888cbf327b4ab857 |
| Source note | uspto-grants-1979_12 |