HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → alpha-Cyano-m-phenoxybenzyl alpha-isopropyl-4-trifluoromethoxyphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)- | HCID 93218 | — |
| Reactant | HCID 20343288 | HCID 20343288 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-Cyano-m-phenoxybenzyl alpha-isopropyl-4-trifluoromethoxyphenylacetate | HCID 54215174 | 39.5% |
Reaction Steps
A solution of α-isopropyl-4-trifluoromethoxyphenylacetyl chloride (4.58 mmol) in ether (5 ml) is added to an ether (20 ml) solution of α-cyano-m-phenoxybenzyl alcohol (4.58 mmol) and pyridine (0.5 ml). The mixture is stirred overnight and filtered. The filtrate and the washings are evaporated and the residual oil is purified on 5×2 mm silica gel plates using 1:1 methylenechloride-hexane as eluent. The band with Rf=0.55 is extracted with ether and evaporated to give the desired ester (0.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04199595 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-beac2b840ec04b7595d15a1d9eee9e1a |
| Source note | uspto-grants-1980_04 |