HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → Fenvalerate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | alpha-Chloro-3-phenoxybenzyl 2-(p-chlorophenyl)-2-isopropyl-acetate | HCID 13061774 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Fenvalerate | HCID 3347 | — |
Reaction Steps
1.5 g of potassium cyanide were added to a mixture of 80 ml of acetonitrile and the solution obtained in Example 9 and the mixture was stirred at 20° C. for 72 hours. Ether was added to the mixture which was then filtered to remove insolubles. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 95-5 cyclohexane-acetone mixture yielded 6.5 g of RS α-cyano-3-phenoxy-benzyl 2-(p-chlorophenyl)-2-isopropyl-acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04315868 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-2f31b6f1604d4bb3b6bbee3da4b9d7e5 |
| Source note | uspto-grants-1982_02 |